Canonical Allele Identifier: PA2828106570
Gene: SAMHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 592135
ClinVar RCV Id: RCV000723336 RCV003489844
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350658.1:p.Ile191Val
CA408822133
NM_001363729.2:c.571A>G