Canonical Allele Identifier: PA104759
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 493373
ClinVar RCV Id: RCV001265185 RCV000585361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Leu131Pro
CA354497998
NM_000539.3:c.392T>C