Canonical Allele Identifier: PA658655104
Gene: RNF213 HGNC NCBI

Linked Data

ClinVar Variation Id: 417841
ClinVar RCV Id: RCV000509629 RCV002525739
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243000.2:p.Pro1721Leu
CA8820321
NM_001256071.3:c.5162C>T