Canonical Allele Identifier: PA645510494
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 437997
ClinVar RCV Id: RCV000505129 RCV000987330 RCV001381860
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Pro170Arg
CA354498718
NM_000539.3:c.509C>G