Allele Registry

Canonical Allele Identifier: PA105687

Gene: SELENON HGNC NCBI

ClinVar RCV:

RCV000004750

ClinVar Variation:

4493

HGVS (amino-acid)	Matching Registered Transcripts
NP_065184.2:p.Trp453Ser	CA253171 NM_020451.3:c.1358G>C