NM_015910.7(WDPCP):c.2063A>G (p.Asn688Ser) AND not specified
- Germline classification:
- Benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000249291.5
Allele description [Variation Report for NM_015910.7(WDPCP):c.2063A>G (p.Asn688Ser)]
NM_015910.7(WDPCP):c.2063A>G (p.Asn688Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens neuromedin U, mRNA (cDNA clone MGC:8934 IMAGE:3864111), complete cd...
Homo sapiens neuromedin U, mRNA (cDNA clone MGC:8934 IMAGE:3864111), complete cdsgi|15277712|gb|BC012908.1|Nucleotide
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Last Updated: Oct 8, 2024