Canonical Allele Identifier: PA2826198716
Gene: PRODH HGNC NCBI
ClinVar RCV:
RCV001053149
ClinVar Variation:
849233
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182155.2:p.Thr358Lys
CA410641923
NM_001195226.2:c.1073C>A