Canonical Allele Identifier: PA126071
Gene: GNAS HGNC NCBI

Linked Data

ClinVar Variation Id: 15934
ClinVar RCV Id: RCV000017290 RCV000017292 RCV000017293 RCV000428995 RCV000429798 RCV000418739 RCV000430768 RCV000436559 RCV000426918 RCV000508670 RCV000419515 RCV000421581 RCV000437187 RCV000439229 RCV000443822 RCV001804738 RCV001813747 RCV004018636
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_536351.1:p.Arg187His
CA126069
NM_080426.4:c.560G>A