Allele Registry

Canonical Allele Identifier: PA2827288962

Gene: CNP HGNC NCBI

ClinVar Allele:

677380

ClinVar RCV:

RCV000850468

RCV004029260

ClinVar Variation:

689708

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317145.1:p.Arg333Trp	CA8569640 NM_001330216.2:c.997C>T