Allele Registry

Canonical Allele Identifier: PA2826617293

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV000627826

ClinVar Variation:

524218

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265846.1:p.Lys305Arg	CA367871485 NM_001278917.2:c.914A>G