Canonical Allele Identifier: PA1139671791
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 870953
ClinVar RCV Id: RCV001090662
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Cys167Trp
CA354498662
NM_000539.3:c.501C>G