Canonical Allele Identifier: PA2573234628
Gene: RGS9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1471896
ClinVar RCV Id: RCV002002764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003826.2:p.Arg501Leu
CA400673407
NM_003835.4:c.1502G>T