Canonical Allele Identifier: PA2825187730
Gene: APRT HGNC NCBI

Linked Data

ClinVar Variation Id: 988059
ClinVar RCV Id: RCV001269451

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000476.1:p.Asp127Gly
CA397087709
NM_000485.3:c.380A>G