Canonical Allele Identifier: PA2826626393
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 863759
ClinVar RCV Id: RCV001070804 RCV002402479
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Phe466Cys
CA346749273
NM_001281492.2:c.1397T>G