Allele Registry

Canonical Allele Identifier: PA105613

Gene: SELENON HGNC NCBI

ClinVar RCV:

RCV000551007

ClinVar Variation:

461629

HGVS (amino-acid)	Matching Registered Transcripts
NP_065184.2:p.Arg469Gln	CA19699053 NM_020451.3:c.1406G>A