Canonical Allele Identifier: PA2826631603
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 135835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ile493Thr
CA010164
NM_001281493.2:c.1478T>C