Canonical Allele Identifier: PA2830514212
Gene: SELENON HGNC NCBI

Linked Data

ClinVar Variation Id: 942173
ClinVar RCV Id: RCV001212108

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996809.1:p.Ala421Ser
CA696838
NM_206926.2:c.1261G>T