Canonical Allele Identifier: PA916018380
Gene: ENTPD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 161579
ClinVar RCV Id: RCV000149114

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278890.1:p.Phe271Tyr
CA174386
NM_001291961.2:c.812T>A