Canonical Allele Identifier: PA104468
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13028
ClinVar RCV Id: RCV000132597 RCV000413771 RCV001074272 RCV000013902 RCV000013903
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Arg135Trp
CA122819
NM_000539.3:c.403C>T