Canonical Allele Identifier: PA105644
Gene: SELENON HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065184.2:p.Gly273Glu
CA253166
NM_020451.3:c.818G>A