Allele Registry

Canonical Allele Identifier: PA102787

Gene: OTC HGNC NCBI

ClinVar RCV:

RCV000083599

ClinVar Variation:

97351

HGVS (amino-acid)	Matching Registered Transcripts
NP_000522.3:p.His302Tyr	CA224824 NM_000531.6:c.904C>T