Canonical Allele Identifier: PA104536
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 1488964
ClinVar RCV Id: RCV001980392
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Cys140Ser
CA354498118
NM_000539.3:c.418T>A
CA354498130
NM_000539.3:c.419G>C