Canonical Allele Identifier: PA916071576
Gene: SELENON HGNC NCBI

Linked Data

ClinVar Variation Id: 95955
ClinVar RCV Id: RCV000558595 RCV000723675 RCV001329140 RCV001097299 RCV003398680 RCV003162515
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996809.1:p.Gly35Arg
CA223578
NM_206926.2:c.103G>C
CA339106029
NM_206926.2:c.103G>A