Canonical Allele Identifier: PA180403
Gene: RP9 HGNC NCBI

Linked Data

ClinVar Variation Id: 167609
ClinVar RCV Id: RCV000153854 RCV000337887 RCV000948763 RCV000987861
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_976033.1:p.Lys210Arg
CA180402
NM_203288.2:c.629A>G