Allele Registry

Canonical Allele Identifier: PA2499241698

Gene: PRODH HGNC NCBI

ClinVar RCV:

RCV001519335

ClinVar Variation:

1168806

HGVS (amino-acid)	Matching Registered Transcripts
NP_001182155.2:p.Trp77Arg	CA10095350 NM_001195226.2:c.229T>C CA410649353 NM_001195226.2:c.229T>A