Canonical Allele Identifier: PA104802
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13043
ClinVar RCV Id: RCV000013918 RCV001075474 RCV004546412
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Met207Arg
CA256686
NM_000539.3:c.620T>G