Canonical Allele Identifier: PA2826198683
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_001182155.2:p.Pro280Leu
CA10095052
NM_001195226.2:c.839C>T