Allele Registry

Canonical Allele Identifier: PA915956938

Gene: CP HGNC NCBI

ClinVar RCV:

RCV000180465

RCV001520185

ClinVar Variation:

198992

HGVS (amino-acid)	Matching Registered Transcripts
NP_000087.2:p.Glu544Asp	CA203697 NM_000096.4:c.1632A>T CA354907329 NM_000096.4:c.1632A>C