Canonical Allele Identifier: PA2826371355
Gene: RNF213 HGNC NCBI

Linked Data

ClinVar Variation Id: 2832568
ClinVar RCV Id: RCV003689576
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243000.2:p.Val4008Gly
CA401409052
NM_001256071.3:c.12023T>G