Canonical Allele Identifier: PA658655113
Gene: RNF213 HGNC NCBI

Linked Data

ClinVar Variation Id: 417850
ClinVar RCV Id: RCV000510103
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243000.2:p.His4051Pro
CA401409334
NM_001256071.3:c.12152A>C