Canonical Allele Identifier: PA2826627253
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 135835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ile665Thr
CA010164
NM_001281492.2:c.1994T>C