Canonical Allele Identifier: PA104656
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 143081
ClinVar RCV Id: RCV000132600 RCV001384606 RCV003888544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Gly188Arg
CA270025
NM_000539.3:c.562G>A
CA354499264
NM_000539.3:c.562G>C