Canonical Allele Identifier: PA104645
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13033
ClinVar RCV Id: RCV001074816 RCV001857346 RCV000013908
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Gly182Ser
CA256679
NM_000539.3:c.544G>A