Canonical Allele Identifier: PA915965049
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 641281
ClinVar RCV Id: RCV000794488
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.His785Asp
CA346753552
NM_000179.3:c.2353C>G