Canonical Allele Identifier: PA104597
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13038
ClinVar RCV Id: RCV000787679 RCV001074389 RCV001207877 RCV000013913
ClinVar Variation Id: 956525
ClinVar RCV Id: RCV001229349
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Gly106Arg
CA256683
NM_000539.3:c.316G>A
CA354496864
NM_000539.3:c.316G>C