Canonical Allele Identifier: PA2580408898
Gene: PRODH HGNC NCBI

Linked Data

ClinVar Variation Id: 2092967
ClinVar RCV Id: RCV003018473
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057419.5:p.Leu515Arg
CA410639160
NM_016335.6:c.1544T>G