Canonical Allele Identifier: PA2826627981
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 821928

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr836Ser
CA346756091
NM_001281492.2:c.2506A>T
CA346756094
NM_001281492.2:c.2507C>G