Canonical Allele Identifier: PA128614
Gene: GNAS HGNC NCBI

Linked Data

ClinVar Variation Id: 29746
ClinVar RCV Id: RCV000022598

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070956.1:p.Leu389Arg
CA128613
NM_001077488.4:c.1166T>G