Allele Registry

Canonical Allele Identifier: PA2573170287

Gene: SELE HGNC NCBI

ClinVar RCV:

RCV002245537

ClinVar Variation:

1684530

HGVS (amino-acid)	Matching Registered Transcripts
NP_000441.2:p.Leu575Phe	CA1235992 NM_000450.2:c.1723C>T