Allele Registry

Canonical Allele Identifier: PA099111

Gene: GNAS HGNC NCBI

ClinVar RCV:

RCV000017306

RCV000595336

RCV001265731

RCV001731308

ClinVar Variation:

15941

HGVS (amino-acid)	Matching Registered Transcripts
NP_000507.1:p.Arg258Trp	CA214672 NM_000516.7:c.772C>T