Canonical Allele Identifier: PA223579
Gene: SELENON HGNC NCBI

Linked Data

ClinVar Variation Id: 95955

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065184.2:p.Gly35Arg
CA223578
NM_020451.3:c.103G>C
CA339106029
NM_020451.3:c.103G>A