Canonical Allele Identifier: PA102969
Gene: GNA11 HGNC NCBI

Linked Data

ClinVar Variation Id: 60666
ClinVar RCV Id: RCV000054479
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002058.2:p.Ser211Trp
CA144608
NM_002067.5:c.632C>G