Canonical Allele Identifier: PA916049343
Gene: PRODH HGNC NCBI

Linked Data

ClinVar Variation Id: 459908
ClinVar RCV Id: RCV000537635 RCV002483383
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057419.5:p.Pro388Leu
CA10095052
NM_016335.6:c.1163C>T