Canonical Allele Identifier: PA112178
Gene: RGS9 HGNC NCBI

Linked Data

ClinVar Variation Id: 5862
ClinVar RCV Id: RCV000006220 RCV000787876 RCV001052039
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003826.2:p.Trp299Arg
CA117815
NM_003835.4:c.895T>C
CA400667416
NM_003835.4:c.895T>A