Canonical Allele Identifier: PA104452
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13024
ClinVar RCV Id: RCV000013898 RCV000256085
ClinVar Variation Id: 279882
ClinVar RCV Id: RCV000299725 RCV001073685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Arg135Leu
CA256671
NM_000539.3:c.404G>T
CA10602881
NM_000539.3:c.404_405delinsTT