Canonical Allele Identifier: PA2826293166
Gene: RNF40 HGNC NCBI

Linked Data

ClinVar Variation Id: 2394002
ClinVar RCV Id: RCV004230504
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193962.1:p.Arg456Cys
CA395683166
NM_001207033.1:c.1366C>T