Allele Registry

Canonical Allele Identifier: PA2825205094

Gene: GNAS HGNC NCBI

ClinVar RCV:

RCV000484773

ClinVar Variation:

419690

HGVS (amino-acid)	Matching Registered Transcripts
NP_000507.1:p.Cys3Ser	CA16620943 NM_000516.7:c.8G>C CA409448626 NM_000516.7:c.7T>A