Allele Registry

Canonical Allele Identifier: PA645440836

Gene: CHRNG HGNC NCBI

ClinVar RCV:

RCV000481365

RCV001141396

RCV001141397

ClinVar Variation:

423846

HGVS (amino-acid)	Matching Registered Transcripts
NP_005190.4:p.Ala44Thr	CA2168512 NM_005199.5:c.130G>A