Canonical Allele Identifier: PA2826198759
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_001182155.2:p.Arg481Trp
CA10094833
NM_001195226.2:c.1441C>T