Canonical Allele Identifier: PA2826939369
Gene: GNAS HGNC NCBI

Linked Data

ClinVar Variation Id: 3029771
ClinVar RCV Id: RCV004531806
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001296771.1:p.Asn14Ser
CA9926874
NM_001309842.2:c.41A>G