Canonical Allele Identifier: PA126072
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
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070956.1:p.Arg202His
CA126069
NM_001077488.4:c.605G>A