Canonical Allele Identifier: PA645508988
Gene: GNAS HGNC NCBI

Linked Data

ClinVar Variation Id: 422467
ClinVar RCV Id: RCV000481496

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070956.1:p.Cys380Tyr
CA16620945
NM_001077488.4:c.1139G>A