Canonical Allele Identifier: PA203831
Gene: RNF216 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

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