Allele Registry

Canonical Allele Identifier: PA2580389967

Gene: CPQ HGNC NCBI

ClinVar RCV:

RCV004123814

ClinVar Variation:

2271948

HGVS (amino-acid)	Matching Registered Transcripts
NP_057218.1:p.Cys233Tyr	CA4817281 NM_016134.4:c.698G>A