Canonical Allele Identifier: PA2826625263
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 921522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser198Ile
CA346741057
NM_001281492.2:c.593G>T