Canonical Allele Identifier: PA658680861
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479867
ClinVar RCV Id: RCV000564228 RCV000688061 RCV000765685 RCV001591322 RCV004000868 RCV003470823
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys728Arg
CA068575
NM_000179.3:c.2183A>G