Canonical Allele Identifier: PA2825313571
Gene: RGR HGNC NCBI

Linked Data

ClinVar Variation Id: 1713538
ClinVar RCV Id: RCV002295541
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001012738.1:p.Ser29Tyr
CA377390589
NM_001012720.2:c.86C>A