Canonical Allele Identifier: PA658813762
Gene: RGS9BP HGNC NCBI

Linked Data

ClinVar Variation Id: 522947
ClinVar RCV Id: RCV000626144 RCV001701422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997274.2:p.Ser122Cys
CA9357532
NM_207391.3:c.365C>G