Canonical Allele Identifier: PA104611
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13022
ClinVar RCV Id: RCV001073422 RCV001857345 RCV000013896
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Gly106Trp
CA256669
NM_000539.3:c.316G>T