Allele Registry

Canonical Allele Identifier: PA101913

Gene: PNP HGNC NCBI

ClinVar Allele:

29029

ClinVar RCV:

RCV000015027

ClinVar Variation:

13990

HGVS (amino-acid)	Matching Registered Transcripts
NP_000261.2:p.Asp128Gly	CA123673 NM_000270.4:c.383A>G