Canonical Allele Identifier: PA205010
Gene: RNF213 HGNC NCBI

Linked Data

ClinVar Variation Id: 210000
ClinVar RCV Id: RCV000191941
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243000.2:p.Arg3922Gln
CA205009
NM_001256071.3:c.11765G>A