Canonical Allele Identifier: PA130466
Gene: RNF213 HGNC NCBI

Linked Data

ClinVar Variation Id: 39701
ClinVar RCV Id: RCV000032903
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243000.2:p.Asp4013Asn
CA130465
NM_001256071.3:c.12037G>A