Canonical Allele Identifier: PA2573317206
Gene: RNF216 HGNC NCBI

Linked Data

ClinVar Variation Id: 1398969
ClinVar RCV Id: RCV001915325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996994.1:p.Arg751His
CA4147861
NM_207111.4:c.2252G>A