Canonical Allele Identifier: PA2830513919
Gene: SELENON HGNC NCBI

Linked Data

ClinVar Variation Id: 212148
ClinVar RCV Id: RCV000193575 RCV000543024 RCV000725931 RCV001097302 RCV002492881
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996809.1:p.Ala105Thr
CA207149
NM_206926.2:c.313G>A