Allele Registry

Canonical Allele Identifier: PA2825482680

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV000486139

ClinVar Variation:

419450

HGVS (amino-acid)	Matching Registered Transcripts
NP_001075224.1:p.Pro211Ser	CA16618557 NM_001081755.3:c.631C>T