Allele Registry

Canonical Allele Identifier: PA645440941

Gene: CHRNG HGNC NCBI

ClinVar Allele:

237286

ClinVar RCV:

RCV000224968

RCV000322027

RCV001094671

RCV004529385

ClinVar Variation:

235605

HGVS (amino-acid)	Matching Registered Transcripts
NP_005190.4:p.Pro506Ser	CA2169080 NM_005199.5:c.1516C>T