Canonical Allele Identifier: PA2830514046
Gene: SELENON HGNC NCBI

Linked Data

ClinVar Variation Id: 2038343
ClinVar RCV Id: RCV002890692
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996809.1:p.Ala240Gly
CA19698400
NM_206926.2:c.719C>G