Canonical Allele Identifier: PA2826628581
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 491952
ClinVar RCV Id: RCV000583381
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly1056Ala
CA346760404
NM_001281492.2:c.3167G>C