Allele Registry

Canonical Allele Identifier: PA2580115335

Gene: SELE HGNC NCBI

ClinVar RCV:

RCV004144009

ClinVar Variation:

2291198

HGVS (amino-acid)	Matching Registered Transcripts
NP_000441.2:p.Ser289Pro	CA343152164 NM_000450.2:c.865T>C