Allele Registry

Canonical Allele Identifier: PA278897

Gene: CHRNG HGNC NCBI

ClinVar RCV:

RCV000020005

RCV003144107

ClinVar Variation:

18338

HGVS (amino-acid)	Matching Registered Transcripts
NP_005190.4:p.Arg101_Pro103dup	CA278896 NM_005199.5:c.301_309dup