Allele Registry

Canonical Allele Identifier: PA915956878

Gene: CP HGNC NCBI

ClinVar RCV:

RCV000034946

ClinVar Variation:

42119

HGVS (amino-acid)	Matching Registered Transcripts
NP_000087.2:p.Pro196Arg	CA344568 NM_000096.4:c.587C>G