Canonical Allele Identifier: PA126066
Gene: GNAS HGNC NCBI

Linked Data

ClinVar Variation Id: 15932
ClinVar RCV Id: RCV000017286 RCV001729350 RCV002288507 RCV002054444
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_536350.2:p.Arg808Cys
CA126062
NM_080425.4:c.2422C>T