Canonical Allele Identifier: PA658815494
Gene: GNAS HGNC NCBI

Linked Data

ClinVar Variation Id: 520563
ClinVar RCV Id: RCV000624712
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057676.1:p.Pro137Ser
CA9926325
NM_016592.5:c.409C>T