Canonical Allele Identifier: PA2741957233
Gene: PRODH HGNC NCBI

Linked Data

ClinVar Variation Id: 3007344
ClinVar RCV Id: RCV003868983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057419.5:p.Trp583Leu
CA410637692
NM_016335.6:c.1748G>T