Canonical Allele Identifier: PA104870
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13050
ClinVar RCV Id: RCV001075386 RCV001381861 RCV001003169 RCV000013925
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Pro171Ser
CA256690
NM_000539.3:c.511C>T