Canonical Allele Identifier: PA2826633673
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127593

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Arg961His
CA014284
NM_001281493.2:c.2882G>A