Canonical Allele Identifier: PA1139723031
Gene: SELENON HGNC NCBI

Linked Data

ClinVar Variation Id: 876389
ClinVar RCV Id: RCV001101131 RCV001373952 RCV004546602 RCV004032076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065184.2:p.Pro432Leu
CA696822
NM_020451.3:c.1295C>T