Allele Registry

Canonical Allele Identifier: PA126810

Gene: SELE HGNC NCBI

ClinVar RCV:

RCV000018147

ClinVar Variation:

16667

HGVS (amino-acid)	Matching Registered Transcripts
NP_000441.2:p.His468Tyr	CA126809 NM_000450.2:c.1402C>T