Canonical Allele Identifier: PA2826628617
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89422

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu1063Lys
CA013478
NM_001281492.2:c.3187G>A