Allele Registry

Canonical Allele Identifier: PA915956885

Gene: CP HGNC NCBI

ClinVar Allele:

51217

ClinVar RCV:

RCV000034879

ClinVar Variation:

42051

HGVS (amino-acid)	Matching Registered Transcripts
NP_000087.2:p.Phe217Ser	CA344481 NM_000096.4:c.650T>C