Canonical Allele Identifier: PA645510492
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 437998
ClinVar RCV Id: RCV000505117 RCV001296378
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Gln28Arg
CA354495583
NM_000539.3:c.83A>G