Canonical Allele Identifier: PA2825091710
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1732314
ClinVar RCV Id: RCV002459367

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg1176Thr
CA346760222
NM_000179.3:c.3527G>C