Allele Registry

Canonical Allele Identifier: PA2826872763

Gene: COA8 HGNC NCBI

ClinVar RCV:

RCV000144488

ClinVar Variation:

156424

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289582.2:p.Glu111del	CA170870 NM_001302653.2:c.331_333del