Canonical Allele Identifier: PA104886
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13013
ClinVar RCV Id: RCV000490234 RCV000763095 RCV001075876 RCV000013887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Pro23His
CA256661
NM_000539.3:c.68C>A