ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA203831
Gene: RNF216
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
196432
ClinVar RCV:
RCV000180793
ClinVar Variation:
199654
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_996994.1:p.Gly456Glu
CA203830
NM_207111.4:c.1367G>A