Allele Registry

Canonical Allele Identifier: PA2580115347

Gene: SELE HGNC NCBI

ClinVar RCV:

RCV004182027

ClinVar Variation:

2345614

HGVS (amino-acid)	Matching Registered Transcripts
NP_000441.2:p.Gln595Glu	CA1235945 NM_000450.2:c.1783C>G