Canonical Allele Identifier: PA2826939263
Gene: GNAS HGNC NCBI

Linked Data

ClinVar Variation Id: 15942
ClinVar RCV Id: RCV000017307

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001296769.1:p.Arg199Ala
CA214677
NM_001309840.2:c.595_596delinsGC