Canonical Allele Identifier: PA159973
Gene: GNAS HGNC NCBI

Linked Data

ClinVar Variation Id: 134496

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_536350.2:p.Ala488Thr
CA159972
NM_080425.4:c.1462G>A