Canonical Allele Identifier: PA2580408927
Gene: PRODH HGNC NCBI

Linked Data

ClinVar Variation Id: 2172236
ClinVar RCV Id: RCV003087325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057419.5:p.Arg598Cys
CA10094831
NM_016335.6:c.1792C>T