Canonical Allele Identifier: PA126059
Gene: GNAS HGNC NCBI

Linked Data

ClinVar Variation Id: 15931
ClinVar RCV Id: RCV000017285
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_536350.2:p.Leu742Pro
CA126057
NM_080425.4:c.2225T>C