Allele Registry

Canonical Allele Identifier: PA645440927

Gene: CHRNG HGNC NCBI

ClinVar RCV:

RCV000275111

RCV001094663

RCV002523122

RCV003327396

RCV004530364

ClinVar Variation:

335007

HGVS (amino-acid)	Matching Registered Transcripts
NP_005190.4:p.Thr310Ser	CA2168866 NM_005199.5:c.928A>T CA351013518 NM_005199.5:c.929C>G