Canonical Allele Identifier: PA645389555
Gene: GNA11 HGNC NCBI

Linked Data

ClinVar Variation Id: 376002
ClinVar RCV Id: RCV000425425 RCV000437415 RCV000444127 RCV002254297 RCV003128401
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002058.2:p.Gln209Leu
CA16602475
NM_002067.5:c.626A>T
CA645607514
NM_002067.5:c.626_627delinsTA
CA645607515
NM_002067.5:c.626_627delinsTT