Canonical Allele Identifier: PA2826371360
Gene: RNF213 HGNC NCBI

Linked Data

ClinVar Variation Id: 2430341
ClinVar RCV Id: RCV003128519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243000.2:p.Cys4017Tyr
CA401409110
NM_001256071.3:c.12050G>A