Canonical Allele Identifier: PA159937
Gene: GNAS HGNC NCBI

Linked Data

ClinVar Variation Id: 134480
ClinVar RCV Id: RCV000121162 RCV002492424 RCV004542876 RCV001547748
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070958.1:p.Leu397Val
CA159936
NM_001077490.3:c.1189C>G