Allele Registry

Canonical Allele Identifier: PA130466

Gene: RNF213 HGNC NCBI

ClinVar RCV:

RCV000032903

ClinVar Variation:

39701

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