Canonical Allele Identifier: PA2826627181
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1054176
ClinVar RCV Id: RCV001362636

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu648His
CA346753381
NM_001281492.2:c.1943T>A