Canonical Allele Identifier: PA2828693440
Gene: RNF216 HGNC NCBI

Linked Data

ClinVar Variation Id: 2466877
ClinVar RCV Id: RCV003196926

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364085.1:p.Arg690Leu
CA4147864
NM_001377156.1:c.2069G>T