Allele Registry

Canonical Allele Identifier: PA916049357

Gene: PRODH HGNC NCBI

ClinVar RCV:

RCV000004214

RCV000004215

RCV000454992

ClinVar Variation:

4006

HGVS (amino-acid)	Matching Registered Transcripts
NP_057419.5:p.Arg453Cys	CA116570 NM_016335.6:c.1357C>T