Canonical Allele Identifier: PA214681
Gene: GNAS HGNC NCBI

Linked Data

ClinVar Variation Id: 15942
ClinVar RCV Id: RCV000017307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070956.1:p.Arg259Ala
CA214677
NM_001077488.4:c.775_776delinsGC