Canonical Allele Identifier: PA2826628949
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127593

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg1133His
CA014284
NM_001281492.2:c.3398G>A