Canonical Allele Identifier: PA099187
Gene: GNAS HGNC NCBI

Linked Data

ClinVar Variation Id: 29746
ClinVar RCV Id: RCV000022598

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000507.1:p.Leu388Arg
CA128613
NM_000516.7:c.1163T>G