Canonical Allele Identifier: PA645465421
Gene: RDX HGNC NCBI

Linked Data

ClinVar Variation Id: 302343

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002897.1:p.Asn502Asp
CA6269961
NM_002906.4:c.1504A>G