Canonical Allele Identifier: PA102958
Gene: GNA11 HGNC NCBI

Linked Data

ClinVar Variation Id: 60664
ClinVar RCV Id: RCV000054477
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002058.2:p.Phe341Leu
CA144606
NM_002067.5:c.1023C>G
CA403312351
NM_002067.5:c.1021T>C
CA403312356
NM_002067.5:c.1023C>A