Canonical Allele Identifier: PA2741816670
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 2831751
ClinVar RCV Id: RCV003686762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Pro171Thr
CA354498720
NM_000539.3:c.511C>A