Canonical Allele Identifier: PA2825313636
Gene: RGR HGNC NCBI

Linked Data

ClinVar Variation Id: 374663
ClinVar RCV Id: RCV000416255
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001012738.1:p.Leu77Arg
CA5581332
NM_001012720.2:c.230T>G