Canonical Allele Identifier: PA105025
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13018
ClinVar RCV Id: RCV000013892 RCV000787682 RCV001002098 RCV001090660 RCV001075619
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Thr17Met
CA256665
NM_000539.3:c.50C>T