Canonical Allele Identifier: PA1139672640
Gene: APRT HGNC NCBI

Linked Data

ClinVar Variation Id: 988060
ClinVar RCV Id: RCV001269452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025189.1:p.Gly133Asp
CA397087556
NM_001030018.2:c.398G>A