Canonical Allele Identifier: PA2573171403
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 1351618
ClinVar RCV Id: RCV002044861
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Ala80Ser
CA354496452
NM_000539.3:c.238G>T