Allele Registry

Canonical Allele Identifier: PA100722

Gene: CHRNG HGNC NCBI

ClinVar Allele:

33379

ClinVar RCV:

RCV000020007

RCV000020008

ClinVar Variation:

18340

HGVS (amino-acid)	Matching Registered Transcripts
NP_005190.4:p.Val107Gly	CA128052 NM_005199.5:c.320T>G