Allele Registry

Canonical Allele Identifier: PA101892

Gene: PNP HGNC NCBI

ClinVar Allele:

29028

ClinVar RCV:

RCV000015026

ClinVar Variation:

13989

HGVS (amino-acid)	Matching Registered Transcripts
NP_000261.2:p.Ala174Pro	CA123671 NM_000270.4:c.520G>C