Canonical Allele Identifier: PA2826625158
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 918559
ClinVar RCV Id: RCV001176217
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr175Pro
CA346740723
NM_001281492.2:c.523A>C