Canonical Allele Identifier: CA122822
Gene: RHO HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 13044
ClinVar RCV Id: RCV000013919
dbSNP Id: rs104893789

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532711C>A , CM000665.2:g.129532711C>A GRCh38
NC_000003.11:g.129251554C>A , CM000665.1:g.129251554C>A GRCh37
NC_000003.10:g.130734244C>A NCBI36
NG_009115.1:g.9073C>A

Transcript Alleles

HGVS Amino-acid change
NM_000539.3:c.875C>A VV NP_000530.1:p.Ala292Glu
ENST00000296271.3:c.875C>A ENSP00000296271.3:p.Ala292Glu