Canonical Allele Identifier: PA104970
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13015
ClinVar RCV Id: RCV000013889 RCV003887861
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Pro347Ser
CA256663
NM_000539.3:c.1039C>T