Canonical Allele Identifier: PA126065
Gene: GNAS HGNC NCBI

Linked Data

ClinVar Variation Id: 15932
ClinVar RCV Id: RCV000017286 RCV001729350 RCV002288507 RCV002054444
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070956.1:p.Arg166Cys
CA126062
NM_001077488.4:c.496C>T