Canonical Allele Identifier: PA105058
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13016
ClinVar RCV Id: RCV001074373 RCV001384460 RCV000013890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Thr58Arg
CA256664
NM_000539.3:c.173C>G