Allele Registry

Canonical Allele Identifier: PA645440936

Gene: CHRNG HGNC NCBI

ClinVar RCV:

RCV000369005

RCV001094622

RCV003765954

ClinVar Variation:

335014

HGVS (amino-acid)	Matching Registered Transcripts
NP_005190.4:p.Asn460Asp	CA2169032 NM_005199.5:c.1378A>G