Canonical Allele Identifier: PA913196123
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 625299
ClinVar RCV Id: RCV000767358 RCV001869053
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Thr62Asn
CA2607080
NM_000539.3:c.185C>A