Allele Registry

Canonical Allele Identifier: PA113645

Gene: APRT HGNC NCBI

ClinVar RCV:

RCV000033903

ClinVar Variation:

18297

HGVS (amino-acid)	Matching Registered Transcripts
NP_000476.1:p.Asp65Val	CA343879 NM_000485.3:c.194A>T