Allele Registry

Canonical Allele Identifier: PA915956968

Gene: CP HGNC NCBI

ClinVar Allele:

51220

ClinVar RCV:

RCV000034882

RCV000334692

RCV000419016

RCV001836633

ClinVar Variation:

42054

HGVS (amino-acid)	Matching Registered Transcripts
NP_000087.2:p.Gly895Ala	CA152494 NM_000096.4:c.2684G>C