Allele Registry

Canonical Allele Identifier: PA2826198702

Gene: PRODH HGNC NCBI

ClinVar RCV:

RCV001774378

ClinVar Variation:

1312924

HGVS (amino-acid)	Matching Registered Transcripts
NP_001182155.2:p.Leu333Gln	CA410642330 NM_001195226.2:c.998T>A