Canonical Allele Identifier: PA645453899
Gene: SELENON HGNC NCBI

Linked Data

ClinVar Variation Id: 280026
ClinVar RCV Id: RCV000358099 RCV000800896 RCV000791286 RCV003985311
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065184.2:p.Arg291Gln
CA696660
NM_020451.3:c.872G>A