Canonical Allele Identifier: PA2825187722
Gene: APRT HGNC NCBI

Linked Data

ClinVar Variation Id: 2179325
ClinVar RCV Id: RCV002615096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000476.1:p.Val125Ile
CA8234431
NM_000485.3:c.373G>A