Canonical Allele Identifier: PA126058
Gene: GNAS HGNC NCBI

Linked Data

ClinVar Variation Id: 15931
ClinVar RCV Id: RCV000017285

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070956.1:p.Leu100Pro
CA126057
NM_001077488.4:c.299T>C