Allele Registry

Canonical Allele Identifier: PA915956935

Gene: CP HGNC NCBI

ClinVar Allele:

207061

ClinVar RCV:

RCV000192950

RCV000398768

RCV001355940

RCV003917744

ClinVar Variation:

210755

HGVS (amino-acid)	Matching Registered Transcripts
NP_000087.2:p.Pro477Leu	CA206118 NM_000096.4:c.1430C>T