NM_000539.3(RHO):c.1034T>C (p.Val345Ala) AND not provided
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Aug 4, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001378537.6
Allele description
NM_000539.3(RHO):c.1034T>C (p.Val345Ala)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens chromosome 18, clone RP11-110H1, complete sequence
Homo sapiens chromosome 18, clone RP11-110H1, complete sequencegi|24796924|gnl|WIBR|L19682|gb|AC10 5|Nucleotide
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See more...Assertion and evidence details
Last Updated: Feb 28, 2024