NM_001276345.2(TNNT2):c.450C>T (p.Ile150=) AND multiple conditions
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Aug 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000867715.9
Allele description [Variation Report for NM_001276345.2(TNNT2):c.450C>T (p.Ile150=)]
NM_001276345.2(TNNT2):c.450C>T (p.Ile150=)
Condition(s)
- Name:
- Hypertrophic cardiomyopathy 2
- Synonyms:
- Familial hypertrophic cardiomyopathy 2; TNNT2-Related Familial Hypertrophic Cardiomyopathy
- Identifiers:
- MONDO: MONDO:0007266; MedGen: C1861864; OMIM: 115195
-
Homo sapiens gravin mRNA, complete cds
Homo sapiens gravin mRNA, complete cdsgi|2218076|gb|U81607.1|HSU81607Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024