Allele Registry

Canonical Allele Identifier: PA210352

Gene: CHRNG HGNC NCBI

ClinVar RCV:

RCV000201797

RCV001775100

RCV003556250

ClinVar Variation:

217751

HGVS (amino-acid)	Matching Registered Transcripts
NP_005190.4:p.Pro143Arg	CA210351 NM_005199.5:c.428C>G