Canonical Allele Identifier: PA2828106823
Gene: SAMHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1469587
ClinVar RCV Id: RCV001973055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350658.1:p.Tyr528Cys
CA9844441
NM_001363729.2:c.1583A>G