Canonical Allele Identifier: PA2580129044
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 1714820
ClinVar RCV Id: RCV002299176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Ala173Val
CA354498754
NM_000539.3:c.518C>T