Canonical Allele Identifier: PA2825187704
Gene: APRT HGNC NCBI

Linked Data

ClinVar Variation Id: 988055
ClinVar RCV Id: RCV001269447 RCV003558782
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000476.1:p.Ile112Phe
CA8234451
NM_000485.3:c.334A>T