Allele Registry

Canonical Allele Identifier: PA2830369493

Gene: COX18 HGNC NCBI

ClinVar RCV:

RCV004168700

ClinVar Variation:

2321831

HGVS (amino-acid)	Matching Registered Transcripts
NP_776188.1:p.His106Asp	CA357199338 NM_173827.4:c.316C>G