Allele Registry

Canonical Allele Identifier: PA915956853

Gene: CP HGNC NCBI

ClinVar RCV:

RCV000034878

RCV003155049

ClinVar Variation:

42050

HGVS (amino-acid)	Matching Registered Transcripts
NP_000087.2:p.Asp77His	CA344479 NM_000096.4:c.229G>C