Canonical Allele Identifier: PA204759
Gene: GNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 208722
ClinVar RCV Id: RCV000190738 RCV000210259 RCV000208571 RCV000225179 RCV000225295 RCV000418135 RCV000755055 RCV001007652 RCV001195548 RCV001255414 RCV001264641 RCV001544504 RCV001795309 RCV002273978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002065.1:p.Ile80Thr
CA204758
NM_002074.5:c.239T>C