Canonical Allele Identifier: PA2826624872
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3230590
ClinVar RCV Id: RCV004520741

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg109Met
CA346740002
NM_001281492.2:c.326G>T