Canonical Allele Identifier: PA174387
Gene: ENTPD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 161579
ClinVar RCV Id: RCV000149114

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001239.2:p.Phe271Tyr
CA174386
NM_001248.4:c.812T>A