Allele Registry

Canonical Allele Identifier: PA915956867

Gene: CP HGNC NCBI

ClinVar RCV:

RCV000034947

ClinVar Variation:

42120

HGVS (amino-acid)	Matching Registered Transcripts
NP_000087.2:p.Gln165Glu	CA344570 NM_000096.4:c.493C>G