Allele Registry

Canonical Allele Identifier: PA123679

Gene: PNP HGNC NCBI

ClinVar RCV:

RCV000015029

RCV000127500

RCV000299797

ClinVar Variation:

13992

HGVS (amino-acid)	Matching Registered Transcripts
NP_000261.2:p.Gly51Ser	CA123677 NM_000270.4:c.151G>A