Allele Registry

Canonical Allele Identifier: PA915956916

Gene: CP HGNC NCBI

ClinVar RCV:

RCV000326860

RCV002520098

RCV003480611

ClinVar Variation:

343779

HGVS (amino-acid)	Matching Registered Transcripts
NP_000087.2:p.Thr313Ile	CA2661194 NM_000096.4:c.938C>T