Canonical Allele Identifier: PA2826939217
Gene: GNAS HGNC NCBI

Linked Data

ClinVar Variation Id: 15937
ClinVar RCV Id: RCV000017297 RCV000017298 RCV000017299 RCV000191991
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001296769.1:p.Arg142Ser
CA126086
NM_001309840.2:c.424C>A