Allele Registry

Canonical Allele Identifier: PA915956895

Gene: CP HGNC NCBI

ClinVar RCV:

RCV000034953

ClinVar Variation:

42126

HGVS (amino-acid)	Matching Registered Transcripts
NP_000087.2:p.Trp283Ser	CA344580 NM_000096.4:c.848G>C