Canonical Allele Identifier: PA2826626689
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 629613
ClinVar RCV Id: RCV000774323 RCV001042028
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr533Ile
CA346750644
NM_001281492.2:c.1598C>T