Canonical Allele Identifier: PA2826625203
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1809567
ClinVar RCV Id: RCV002481146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg186Thr
CA346740803
NM_001281492.2:c.557G>C