Canonical Allele Identifier: PA2580408900
Gene: PRODH HGNC NCBI

Linked Data

ClinVar Variation Id: 1938923
ClinVar RCV Id: RCV002666547
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057419.5:p.His520Tyr
CA10094888
NM_016335.6:c.1558C>T