Allele Registry

Canonical Allele Identifier: PA2826939357

Gene: GNAS HGNC NCBI

ClinVar RCV:

RCV000484773

ClinVar Variation:

419690

HGVS (amino-acid)	Matching Registered Transcripts
NP_001296771.1:p.Cys3Ser	CA16620943 NM_001309842.2:c.8G>C CA409448626 NM_001309842.2:c.7T>A