Canonical Allele Identifier: PA105098
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13052
ClinVar RCV Id: RCV000013927 RCV001213632
ClinVar Variation Id: 636081
ClinVar RCV Id: RCV000787676 RCV001042727
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Val345Leu
CA256693
NM_000539.3:c.1033G>C
CA354471268
NM_000539.3:c.1033G>T