Canonical Allele Identifier: PA2826198717
Gene: PRODH HGNC NCBI

Linked Data

ClinVar Variation Id: 4013
ClinVar RCV Id: RCV000004228 RCV000004227 RCV002225259
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182155.2:p.Thr358Met
CA116582
NM_001195226.2:c.1073C>T