Canonical Allele Identifier: PA126087
Gene: GNAS HGNC NCBI

Linked Data

ClinVar Variation Id: 15937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070956.1:p.Arg202Ser
CA126086
NM_001077488.4:c.604C>A