Allele Registry

Canonical Allele Identifier: PA2826198717

Gene: PRODH HGNC NCBI

ClinVar RCV:

RCV000004227

RCV000004228

RCV002225259

ClinVar Variation:

4013

HGVS (amino-acid)	Matching Registered Transcripts
NP_001182155.2:p.Thr358Met	CA116582 NM_001195226.2:c.1073C>T