Allele Registry

Canonical Allele Identifier: PA2825187754

Gene: APRT HGNC NCBI

ClinVar RCV:

RCV000019964

ClinVar Variation:

18302

HGVS (amino-acid)	Matching Registered Transcripts
NP_000476.1:p.Ter181Ser	CA258149 NM_000485.3:c.542G>C