Allele Registry

Canonical Allele Identifier: PA102969

Gene: GNA11 HGNC NCBI

ClinVar RCV:

RCV000054479

ClinVar Variation:

60666

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