Canonical Allele Identifier: PA2826624891
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1758054
ClinVar RCV Id: RCV002382629

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg113Gly
CA346740024
NM_001281492.2:c.337C>G