Canonical Allele Identifier: PA104938
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13032
ClinVar RCV Id: RCV000013907 RCV001003173 RCV001382064
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Pro347Arg
CA256678
NM_000539.3:c.1040C>G