Canonical Allele Identifier: PA223587
Gene: SELENON HGNC NCBI

Linked Data

ClinVar Variation Id: 95961
ClinVar RCV Id: RCV000542565 RCV000723596 RCV001097379 RCV001329142 RCV003398681
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065184.2:p.Glu552Lys
CA223586
NM_020451.3:c.1654G>A