Canonical Allele Identifier: PA915964851
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 655827
ClinVar RCV Id: RCV000812085 RCV002424910
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val717Phe
CA346751107
NM_000179.3:c.2149G>T