Allele Registry

Canonical Allele Identifier: PA2826198709

Gene: PRODH HGNC NCBI

ClinVar RCV:

RCV000004220

RCV000004221

RCV001227275

RCV002512744

RCV003430632

ClinVar Variation:

4009

954759

HGVS (amino-acid)	Matching Registered Transcripts
NP_001182155.2:p.Ala347Ser	CA116576 NM_001195226.2:c.1039G>T CA1139666956 NM_001195226.2:c.1038_1039delinsAT