Canonical Allele Identifier: PA299497
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 36596

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys13Thr
CA014649
NM_000179.3:c.38A>C