Canonical Allele Identifier: PA916049355
Gene: PRODH HGNC NCBI

Linked Data

ClinVar Variation Id: 4008
ClinVar RCV Id: RCV000004219 RCV000004218 RCV000412946 RCV002512743
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057419.5:p.Leu441Pro
CA116574
NM_016335.6:c.1322T>C