Allele Registry

Canonical Allele Identifier: PA105672

Gene: SELENON HGNC NCBI

ClinVar RCV:

RCV000349806

RCV002520484

ClinVar Variation:

297025

HGVS (amino-acid)	Matching Registered Transcripts
NP_065184.2:p.His293Arg	CA696675 NM_020451.3:c.878A>G