Allele Registry

Canonical Allele Identifier: PA2825481851

Gene: ELN HGNC NCBI

ClinVar Variation Id: 360635

HGVS (amino-acid)	Matching Registered Transcripts
NP_001075222.1:p.Phe87Leu	CA4292410 NM_001081753.3:c.259T>C CA367869203 NM_001081753.3:c.261T>A CA367869204 NM_001081753.3:c.261T>G