Allele Registry

Canonical Allele Identifier: PA2826615550

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV000627826

ClinVar Variation:

524218

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265842.1:p.Lys279Arg	CA367871485 NM_001278913.2:c.836A>G