Allele Registry

Canonical Allele Identifier: PA2829863426

Gene: PRODH HGNC NCBI

ClinVar RCV:

RCV001519335

ClinVar Variation:

1168806

HGVS (amino-acid)	Matching Registered Transcripts
NP_057419.5:p.Trp185Arg	CA10095350 NM_016335.6:c.553T>C CA410649353 NM_016335.6:c.553T>A