Allele Registry

Canonical Allele Identifier: PA2580190011

Gene: COX18 HGNC NCBI

ClinVar RCV:

RCV004168700

ClinVar Variation:

2321831

HGVS (amino-acid)	Matching Registered Transcripts
NP_001287658.1:p.Ser142Arg	CA357199337 NM_001300729.1:c.426C>A CA357199338 NM_001300729.1:c.426C>G CA357199344 NM_001300729.1:c.424A>C