Allele Registry

Canonical Allele Identifier: PA915956939

Gene: CP HGNC NCBI

ClinVar RCV:

RCV000034952

RCV000116816

RCV001539064

ClinVar Variation:

42125

HGVS (amino-acid)	Matching Registered Transcripts
NP_000087.2:p.Thr551Ile	CA152488 NM_000096.4:c.1652C>T