Canonical Allele Identifier: PA2826625100
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2567482

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser162Arg
CA346740646
NM_001281492.2:c.484A>C
CA346740655
NM_001281492.2:c.486C>A
CA346740656
NM_001281492.2:c.486C>G