Canonical Allele Identifier: PA104625
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 866181
ClinVar RCV Id: RCV001073984 RCV001265179 RCV001862531
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Gly109Arg
CA354496896
NM_000539.3:c.325G>A
CA354496901
NM_000539.3:c.325G>C