Allele Registry

Canonical Allele Identifier: PA2830526450

Gene: RNF216 HGNC NCBI

ClinVar RCV:

RCV000180793

ClinVar Variation:

199654

HGVS (amino-acid)	Matching Registered Transcripts
NP_996999.1:p.Gly399Glu	CA203830 NM_207116.3:c.1196G>A