Canonical Allele Identifier: PA2830514047
Gene: SELENON HGNC NCBI

Linked Data

ClinVar Variation Id: 2412645
ClinVar RCV Id: RCV002789938
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996809.1:p.Ala240Pro
CA696649
NM_206926.2:c.718G>C