ClinGen Allele Registry
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Canonical Allele Identifier:
PA916049305
Gene: PRODH
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000004216
RCV000004217
RCV001577052
RCV001731278
ClinVar Variation:
4007
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_057419.5:p.Leu289Met
CA116572
NM_016335.6:c.865T>A