Canonical Allele Identifier: PA104501
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13026
ClinVar RCV Id: RCV000013900 RCV001386998 RCV003887863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Asp190Gly
CA256673
NM_000539.3:c.569A>G