Canonical Allele Identifier: PA102645
Gene: OTC HGNC NCBI

Linked Data

ClinVar Variation Id: 97117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000522.3:p.Gly50Arg
CA224471
NM_000531.6:c.148G>A
CA412716119
NM_000531.6:c.148G>C