Canonical Allele Identifier: PA2828107075
Gene: SAMHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 425269
ClinVar RCV Id: RCV000488134

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350662.1:p.His129Asp
CA16621789
NM_001363733.2:c.385C>G