Canonical Allele Identifier: PA916073949
Gene: RNF216 HGNC NCBI

Linked Data

ClinVar Variation Id: 800990
ClinVar RCV Id: RCV000985218
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996994.1:p.Val888Glu
CA366730973
NM_207111.4:c.2663T>A