Canonical Allele Identifier: PA104920
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13034
ClinVar RCV Id: RCV000013909 RCV001003172 RCV001582479
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Pro267Leu
CA256680
NM_000539.3:c.800C>T