Allele Registry

Canonical Allele Identifier: PA645440851

Gene: CHRNG HGNC NCBI

ClinVar RCV:

RCV000302205

RCV001094611

RCV003765950

ClinVar Variation:

335002

HGVS (amino-acid)	Matching Registered Transcripts
NP_005190.4:p.Glu123Lys	CA2168646 NM_005199.5:c.367G>A