Canonical Allele Identifier: PA2580408919
Gene: PRODH HGNC NCBI

Linked Data

ClinVar Variation Id: 2225230
ClinVar RCV Id: RCV002683789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057419.5:p.Arg589Trp
CA10094833
NM_016335.6:c.1765C>T