Allele Registry

Canonical Allele Identifier: PA2580115320

Gene: SELE HGNC NCBI

ClinVar RCV:

RCV004275832

ClinVar Variation:

2489239

HGVS (amino-acid)	Matching Registered Transcripts
NP_000441.2:p.Lys76Arg	CA343157111 NM_000450.2:c.227A>G