Canonical Allele Identifier: PA2830514044
Gene: SELENON HGNC NCBI

Linked Data

ClinVar Variation Id: 4489
ClinVar RCV Id: RCV000004746
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996809.1:p.Gly239Glu
CA253166
NM_206926.2:c.716G>A