Canonical Allele Identifier: PA913196121
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 625297
ClinVar RCV Id: RCV000767356 RCV001003166 RCV001366656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Gly18Asp
CA2607047
NM_000539.3:c.53G>A