Canonical Allele Identifier: PA2826634848
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1502499
ClinVar RCV Id: RCV002045184

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ala198Glu
CA346746196
NM_001281494.2:c.593C>A