Canonical Allele Identifier: PA2741826323
Gene: APRT HGNC NCBI

Linked Data

ClinVar Variation Id: 2538840
ClinVar RCV Id: RCV003261529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025189.1:p.Ala116Val
CA8234445
NM_001030018.2:c.347C>T