Canonical Allele Identifier: PA2826371354
Gene: RNF213 HGNC NCBI

Linked Data

ClinVar Variation Id: 2444199
ClinVar RCV Id: RCV003152997
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243000.2:p.Cys4000Tyr
CA401408998
NM_001256071.3:c.11999G>A