Canonical Allele Identifier: PA159935
Gene: GNAS HGNC NCBI

Linked Data

ClinVar Variation Id: 134479

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070958.1:p.Pro374Thr
CA159934
NM_001077490.3:c.1120C>A