Canonical Allele Identifier: PA214682
Gene: GNAS HGNC NCBI

Linked Data

ClinVar Variation Id: 15942
ClinVar RCV Id: RCV000017307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_536350.2:p.Arg901Ala
CA214677
NM_080425.4:c.2701_2702delinsGC