Allele Registry

Canonical Allele Identifier: PA113692

Gene: APRT HGNC NCBI

ClinVar RCV:

RCV000033909

ClinVar Variation:

41012

HGVS (amino-acid)	Matching Registered Transcripts
NP_000476.1:p.Val150Phe	CA343887 NM_000485.3:c.448G>T