Canonical Allele Identifier: PA1139672596
Gene: APRT HGNC NCBI

Linked Data

ClinVar Variation Id: 988056
ClinVar RCV Id: RCV001269448 RCV003558783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025189.1:p.Glu118Gln
CA8234444
NM_001030018.2:c.352G>C