Canonical Allele Identifier: PA214680
Gene: GNAS HGNC NCBI

Linked Data

ClinVar Variation Id: 15942
ClinVar RCV Id: RCV000017307

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000507.1:p.Arg258Ala
CA214677
NM_000516.7:c.772_773delinsGC