Canonical Allele Identifier: PA104950
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13053
ClinVar RCV Id: RCV000013928 RCV001851840
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Pro347Gln
CA256694
NM_000539.3:c.1040C>A