Canonical Allele Identifier: PA2573269327
Gene: SAMHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1379468
ClinVar RCV Id: RCV001914862
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056289.2:p.Pro187Thr
CA408822189
NM_015474.4:c.559C>A