Allele Registry

Canonical Allele Identifier: PA916076328

Gene: CNP HGNC NCBI

ClinVar Allele:

677380

ClinVar RCV:

RCV000850468

RCV004029260

ClinVar Variation:

689708

HGVS (amino-acid)	Matching Registered Transcripts
NP_149124.3:p.Arg353Trp	CA8569640 NM_033133.5:c.1057C>T