Canonical Allele Identifier: PA2826625255
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 184803

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr197Ser
CA016745
NM_001281492.2:c.590C>G
CA346741015
NM_001281492.2:c.589A>T