Canonical Allele Identifier: PA104635
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13048
ClinVar RCV Id: RCV000013923 RCV001851839
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Gly114Asp
CA256688
NM_000539.3:c.341G>A