Allele Registry

Canonical Allele Identifier: PA915957440

Gene: APRT HGNC NCBI

ClinVar Allele:

33339

ClinVar RCV:

RCV000019962

ClinVar Variation:

18300

HGVS (amino-acid)	Matching Registered Transcripts
NP_001025189.1:p.Leu110Pro	CA258148 NM_001030018.2:c.329T>C