Allele Registry

Canonical Allele Identifier: PA2741817641

Gene: SELE HGNC NCBI

ClinVar Allele:

2782404

ClinVar RCV:

RCV004365141

ClinVar Variation:

2618659

HGVS (amino-acid)	Matching Registered Transcripts
NP_000441.2:p.Met279Thr	CA32480796 NM_000450.2:c.836T>C