Canonical Allele Identifier: PA2580524831
Gene: RNF168 HGNC NCBI

Linked Data

ClinVar Variation Id: 2265091
ClinVar RCV Id: RCV002808598
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689830.2:p.Arg165Gly
CA355625235
NM_152617.4:c.493C>G