Canonical Allele Identifier: PA113662
Gene: APRT HGNC NCBI

Linked Data

ClinVar Variation Id: 988060
ClinVar RCV Id: RCV001269452
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000476.1:p.Gly133Asp
CA397087556
NM_000485.3:c.398G>A