Canonical Allele Identifier: PA2825187732
Gene: APRT HGNC NCBI

Linked Data

ClinVar Variation Id: 988063
ClinVar RCV Id: RCV001269455

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000476.1:p.Leu130Pro
CA397087624
NM_000485.3:c.389T>C