Canonical Allele Identifier: PA2741816668
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 2628035
ClinVar RCV Id: RCV003389585

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Met163Ile
CA2607172
NM_000539.3:c.489G>A
CA354498561
NM_000539.3:c.489G>T
CA354498564
NM_000539.3:c.489G>C