ClinGen Allele Registry
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Canonical Allele Identifier:
PA916049300
Gene: PRODH
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000287188
RCV001519336
RCV001651301
ClinVar Variation:
281129
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_057419.5:p.Pro30Ser
CA10095503
NM_016335.6:c.88C>T