Canonical Allele Identifier: PA102897
Gene: OTC HGNC NCBI

Linked Data

ClinVar Variation Id: 11008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000522.3:p.Leu304Phe
CA224834
NM_000531.6:c.912G>T
CA412725911
NM_000531.6:c.912G>C