Allele Registry

Canonical Allele Identifier: PA205024

Gene: RNF213 HGNC NCBI

ClinVar RCV:

RCV000191948

RCV000879574

ClinVar Variation:

210007

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243000.2:p.Arg4019Cys	CA205023 NM_001256071.3:c.12055C>T