Allele Registry

Canonical Allele Identifier: PA916049361

Gene: PRODH HGNC NCBI

ClinVar RCV:

RCV000004227

RCV000004228

RCV002225259

ClinVar Variation:

4013

HGVS (amino-acid)	Matching Registered Transcripts
NP_057419.5:p.Thr466Met	CA116582 NM_016335.6:c.1397C>T