Canonical Allele Identifier: PA2828106543
Gene: SAMHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2240985
ClinVar RCV Id: RCV002719367

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350658.1:p.Phe165Leu
CA408822806
NM_001363729.2:c.495T>G
CA408822807
NM_001363729.2:c.495T>A
CA408822819
NM_001363729.2:c.493T>C