Canonical Allele Identifier: PA274820
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 135835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile795Thr
CA010164
NM_000179.3:c.2384T>C