Canonical Allele Identifier: PA103089
Gene: OTC HGNC NCBI

Linked Data

ClinVar Variation Id: 97273

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000522.3:p.Ser207Arg
CA224715
NM_000531.6:c.621C>A
CA412725703
NM_000531.6:c.619A>C
CA412725721
NM_000531.6:c.621C>G