Allele Registry

Canonical Allele Identifier: PA915956966

Gene: CP HGNC NCBI

ClinVar RCV:

RCV000034881

ClinVar Variation:

42053

HGVS (amino-acid)	Matching Registered Transcripts
NP_000087.2:p.Gly892Glu	CA344485 NM_000096.4:c.2675G>A