Canonical Allele Identifier: PA130464
Gene: RNF213 HGNC NCBI

Linked Data

ClinVar Variation Id: 39700
ClinVar RCV Id: RCV000032902 RCV001531872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243000.2:p.Arg4810Lys
CA130463
NM_001256071.3:c.14429G>A