Allele Registry

Canonical Allele Identifier: PA2825481859

Gene: ELN HGNC NCBI

ClinVar Variation Id: 213171

HGVS (amino-acid)	Matching Registered Transcripts
NP_001075222.1:p.Gly109Asp	CA320313 NM_001081753.3:c.326G>A