Canonical Allele Identifier: PA2826627982
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1384959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr836Ile
CA346756096
NM_001281492.2:c.2507C>T