Canonical Allele Identifier: PA658655109
Gene: RNF213 HGNC NCBI

Linked Data

ClinVar Variation Id: 417846
ClinVar RCV Id: RCV000509672 RCV001261790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243000.2:p.His4014Asn
CA401409087
NM_001256071.3:c.12040C>A