Allele Registry

Canonical Allele Identifier: PA915956963

Gene: CP HGNC NCBI

ClinVar RCV:

RCV000364282

RCV000514945

RCV003912452

ClinVar Variation:

343753

HGVS (amino-acid)	Matching Registered Transcripts
NP_000087.2:p.Asp871Asn	CA2660675 NM_000096.4:c.2611G>A