Canonical Allele Identifier: PA097939
Gene: SAMHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 126412

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056289.2:p.Arg145Gln
CA345523
NM_015474.4:c.434G>A