Canonical Allele Identifier: PA2580569872
Gene: RNF216 HGNC NCBI

Linked Data

ClinVar Variation Id: 2466877
ClinVar RCV Id: RCV003196926

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996994.1:p.Arg747Leu
CA4147864
NM_207111.4:c.2240G>T