Canonical Allele Identifier: PA2499233108
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 1049601
ClinVar RCV Id: RCV001355933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Ile307Phe
CA2607310
NM_000539.3:c.919A>T