Allele Registry

Canonical Allele Identifier: PA645440935

Gene: CHRNG HGNC NCBI

ClinVar RCV:

RCV000311936

RCV001094621

RCV003765953

ClinVar Variation:

335013

HGVS (amino-acid)	Matching Registered Transcripts
NP_005190.4:p.Pro420Leu	CA2169009 NM_005199.5:c.1259C>T