Canonical Allele Identifier: PA2580445509
Gene: SELENON HGNC NCBI

Linked Data

ClinVar Variation Id: 2038343
ClinVar RCV Id: RCV002890692

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065184.2:p.Ala274Gly
CA19698400
NM_020451.3:c.821C>G