Canonical Allele Identifier: PA256696
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13055
ClinVar RCV Id: RCV000013930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Pro23Ala
CA256695
NM_000539.3:c.67C>G