Canonical Allele Identifier: PA104443
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 1456261
ClinVar RCV Id: RCV001946834
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Arg135Gly
CA354498053
NM_000539.3:c.403C>G