Canonical Allele Identifier: PA2826626395
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479879
ClinVar RCV Id: RCV000568285 RCV000629691 RCV001821658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Phe466Tyr
CA346749269
NM_001281492.2:c.1397T>A