Canonical Allele Identifier: PA2828106569
Gene: SAMHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1470785
ClinVar RCV Id: RCV001995305
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350658.1:p.Ile191Leu
CA408822131
NM_001363729.2:c.571A>T
CA408822135
NM_001363729.2:c.571A>C