Canonical Allele Identifier: PA105119
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13020
ClinVar RCV Id: RCV000013894 RCV001198366
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Val87Asp
CA256667
NM_000539.3:c.260T>A