Allele Registry

Canonical Allele Identifier: PA2741817639

Gene: SELE HGNC NCBI

ClinVar RCV:

RCV004314885

ClinVar Variation:

2545148

HGVS (amino-acid)	Matching Registered Transcripts
NP_000441.2:p.Ala249Ser	CA32480881 NM_000450.2:c.745G>T