Allele Registry

Canonical Allele Identifier: PA126065

Gene: GNAS HGNC NCBI

ClinVar Allele:

30971

ClinVar RCV:

RCV000017286

RCV001729350

RCV002054444

RCV002288507

ClinVar Variation:

15932

HGVS (amino-acid)	Matching Registered Transcripts
NP_001070956.1:p.Arg166Cys	CA126062 NM_001077488.4:c.496C>T