Canonical Allele Identifier: PA916049300
Gene: PRODH HGNC NCBI

Linked Data

ClinVar Variation Id: 281129
ClinVar RCV Id: RCV000287188 RCV001519336 RCV001651301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057419.5:p.Pro30Ser
CA10095503
NM_016335.6:c.88C>T