Allele Registry

Canonical Allele Identifier: PA915956929

Gene: CP HGNC NCBI

ClinVar RCV:

RCV000260851

RCV001770276

RCV002520097

ClinVar Variation:

343773

HGVS (amino-acid)	Matching Registered Transcripts
NP_000087.2:p.Ala406Glu	CA2661092 NM_000096.4:c.1217C>A