Canonical Allele Identifier: PA2826626727
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479877

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr542Ile
CA346750694
NM_001281492.2:c.1625C>T