Canonical Allele Identifier: PA097967
Gene: SAMHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 4066
ClinVar RCV Id: RCV000004281
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056289.2:p.Gly209Ser
CA340140
NM_015474.4:c.625G>A