Canonical Allele Identifier: PA2825483235
Gene: RGS9 HGNC NCBI

Linked Data

ClinVar Variation Id: 94379
ClinVar RCV Id: RCV000080351 RCV001519931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075424.1:p.Arg498His
CA147787
NM_001081955.3:c.1493G>A