Canonical Allele Identifier: PA2826627772
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 480919
ClinVar RCV Id: RCV000561147 RCV000590239 RCV000793228 RCV003459309 RCV004000907
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala785Gly
CA346755403
NM_001281492.2:c.2354C>G