Allele Registry

Canonical Allele Identifier: PA118049

Gene: COX15 HGNC NCBI

ClinVar RCV:

RCV000006551

RCV001553427

RCV002512834

ClinVar Variation:

6175

HGVS (amino-acid)	Matching Registered Transcripts
NP_004367.2:p.Arg217Trp	CA118046 NM_004376.7:c.649C>T