Allele Registry

Canonical Allele Identifier: PA203831

Gene: RNF216 HGNC NCBI

ClinVar RCV:

RCV000180793

ClinVar Variation:

199654

HGVS (amino-acid)	Matching Registered Transcripts
NP_996994.1:p.Gly456Glu	CA203830 NM_207111.4:c.1367G>A