Canonical Allele Identifier: PA170732
Gene: GNA11 HGNC NCBI

Linked Data

ClinVar Variation Id: 155926
ClinVar RCV Id: RCV000144048
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002058.2:p.Arg60Leu
CA170731
NM_002067.5:c.179G>T