Canonical Allele Identifier: PA1139674851
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 932699
ClinVar RCV Id: RCV001200627

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp763Ala
CA346752937
NM_000179.3:c.2288A>C