Canonical Allele Identifier: PA126068
Gene: GNAS HGNC NCBI

Linked Data

ClinVar Variation Id: 15933
ClinVar RCV Id: RCV000017287 RCV000017289 RCV000133503 RCV000422043 RCV000427542 RCV000431495 RCV000432295 RCV000421422 RCV000444862 RCV000429524 RCV000437784 RCV000443647 RCV000420084 RCV000439728 RCV000508635 RCV002513071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070956.1:p.Arg202Cys
CA126067
NM_001077488.4:c.604C>T