Allele Registry

Canonical Allele Identifier: PA915956940

Gene: CP HGNC NCBI

ClinVar Allele:

411511

ClinVar RCV:

RCV000487430

ClinVar Variation:

424620

HGVS (amino-acid)	Matching Registered Transcripts
NP_000087.2:p.Cys560Phe	CA16621520 NM_000096.4:c.1679G>T