Canonical Allele Identifier: PA1139675135
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 847677
ClinVar RCV Id: RCV001051274 RCV003307860
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser806Thr
CA346754000
NM_000179.3:c.2416T>A