Canonical Allele Identifier: PA2580128898
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 2001823
ClinVar RCV Id: RCV002815736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Ile75Val
CA2607093
NM_000539.3:c.223A>G