Canonical Allele Identifier: PA2830514287
Gene: SELENON HGNC NCBI

Linked Data

ClinVar Variation Id: 95961

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996809.1:p.Glu518Lys
CA223586
NM_206926.2:c.1552G>A