Canonical Allele Identifier: PA2580128953
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 2060137
ClinVar RCV Id: RCV002957536
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Cys110Trp
CA354496922
NM_000539.3:c.330C>G