Canonical Allele Identifier: PA2826629162
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala1172Thr
CA346761429
NM_001281492.2:c.3514G>A