Canonical Allele Identifier: PA2826939637
Gene: GNAS HGNC NCBI

Linked Data

ClinVar Variation Id: 422467
ClinVar RCV Id: RCV000481496

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001296790.1:p.Cys320Tyr
CA16620945
NM_001309861.2:c.959G>A