Allele Registry

Canonical Allele Identifier: PA916049360

Gene: PRODH HGNC NCBI

ClinVar RCV:

RCV000004220

RCV000004221

RCV001227275

RCV002512744

RCV003430632

ClinVar Variation:

4009

954759

HGVS (amino-acid)	Matching Registered Transcripts
NP_057419.5:p.Ala455Ser	CA116576 NM_016335.6:c.1363G>T CA1139666956 NM_016335.6:c.1362_1363delinsAT