Canonical Allele Identifier: PA1139672637
Gene: APRT HGNC NCBI

Linked Data

ClinVar Variation Id: 988059
ClinVar RCV Id: RCV001269451

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025189.1:p.Asp127Gly
CA397087709
NM_001030018.2:c.380A>G