Canonical Allele Identifier: PA207150
Gene: SELENON HGNC NCBI

Linked Data

ClinVar Variation Id: 212148

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065184.2:p.Ala139Thr
CA207149
NM_020451.3:c.415G>A