Canonical Allele Identifier: PA253169
Gene: SELENON HGNC NCBI

Linked Data

ClinVar Variation Id: 4491
ClinVar RCV Id: RCV000004748 RCV000482307 RCV002288464 RCV002504747
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065184.2:p.Met1Val