Allele Registry

Canonical Allele Identifier: PA645440814

Gene: CHRNG HGNC NCBI

ClinVar RCV:

RCV000420882

RCV001138817

RCV001138818

RCV001354901

RCV004544730

ClinVar Variation:

376837

HGVS (amino-acid)	Matching Registered Transcripts
NP_005190.4:p.Arg42Gln	CA2168508 NM_005199.5:c.125G>A