Canonical Allele Identifier: PA2826626419
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2165988
ClinVar RCV Id: RCV003090265
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys473Glu
CA346749367
NM_001281492.2:c.1417A>G