Canonical Allele Identifier: PA102338
Gene: OTC HGNC NCBI

Linked Data

ClinVar Variation Id: 10999

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000522.3:p.Arg277Trp
CA255648
NM_000531.6:c.829C>T