Allele Registry

Canonical Allele Identifier: PA915969830

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV000627826

ClinVar Variation:

524218

HGVS (amino-acid)	Matching Registered Transcripts
NP_001075223.1:p.Lys320Arg	CA367871485 NM_001081754.3:c.959A>G