Canonical Allele Identifier: PA2826626866
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2453196
ClinVar RCV Id: RCV003182651
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala574Asp
CA346750944
NM_001281492.2:c.1721C>A