Canonical Allele Identifier: PA1139672146
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 853413
ClinVar RCV Id: RCV001058214
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Pro267Thr
CA354470391
NM_000539.3:c.799C>A