Allele Registry

Canonical Allele Identifier: PA915957437

Gene: APRT HGNC NCBI

ClinVar Allele:

33336

ClinVar RCV:

RCV000033903

ClinVar Variation:

18297

HGVS (amino-acid)	Matching Registered Transcripts
NP_001025189.1:p.Asp65Val	CA343879 NM_001030018.2:c.194A>T