Canonical Allele Identifier: PA128616
Gene: GNAS HGNC NCBI

Linked Data

ClinVar Variation Id: 29747
ClinVar RCV Id: RCV000022599 RCV000174485
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070956.1:p.Glu393Lys
CA128615
NM_001077488.4:c.1177G>A