Canonical Allele Identifier: PA276996
Gene: SELENON HGNC NCBI

Linked Data

ClinVar Variation Id: 212149
ClinVar RCV Id: RCV000192616 RCV000599220 RCV003338457 RCV002517132
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065184.2:p.Ala276_Cys277insSer
CA276995
NM_020451.3:c.827_829dup