Canonical Allele Identifier: PA1139671631
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 935773
ClinVar RCV Id: RCV001204435
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Leu77Phe
CA354496411
NM_000539.3:c.229C>T