Canonical Allele Identifier: PA1139671825
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 964188
ClinVar RCV Id: RCV001238364
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Ala173Thr
CA2607180
NM_000539.3:c.517G>A