Canonical Allele Identifier: PA2826939342
Gene: GNAS HGNC NCBI

Linked Data

ClinVar Variation Id: 29746
ClinVar RCV Id: RCV000022598

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001296769.1:p.Leu329Arg
CA128613
NM_001309840.2:c.986T>G