Canonical Allele Identifier: PA2826939300
Gene: GNAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1215279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001296769.1:p.Gly270Arg
CA409453548
NM_001309840.2:c.808G>A
CA409453549
NM_001309840.2:c.808G>C