Canonical Allele Identifier: PA645454811
Gene: SELENON HGNC NCBI

Linked Data

ClinVar Variation Id: 281048
ClinVar RCV Id: RCV000340120 RCV001083468 RCV000723478 RCV000765103 RCV003920033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065184.2:p.Thr572Asn
CA696975
NM_020451.3:c.1715C>A