Canonical Allele Identifier: PA113669
Gene: APRT HGNC NCBI
ClinVar RCV:
RCV000019962
ClinVar Variation:
18300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000476.1:p.Leu110Pro
CA258148
NM_000485.3:c.329T>C