Canonical Allele Identifier: PA2573171398
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 1366909
ClinVar RCV Id: RCV001932362
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Val49Met
CA2607069
NM_000539.3:c.145G>A