Canonical Allele Identifier: PA159921
Gene: GNA11 HGNC NCBI

Linked Data

ClinVar Variation Id: 134472
ClinVar RCV Id: RCV000121154 RCV000889157
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002058.2:p.Ala65Thr
CA159920
NM_002067.5:c.193G>A