Canonical Allele Identifier: PA915957437
Gene: APRT HGNC NCBI

Linked Data

ClinVar Variation Id: 18297
ClinVar RCV Id: RCV000033903
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025189.1:p.Asp65Val
CA343879
NM_001030018.2:c.194A>T