Canonical Allele Identifier: PA913196128
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 625301
ClinVar RCV Id: RCV000767360 RCV003558565
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Gly101Val
CA354496798
NM_000539.3:c.302G>T