Allele Registry

Canonical Allele Identifier: PA2826616868

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV000627826

ClinVar Variation:

524218

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265845.1:p.Lys301Arg	CA367871485 NM_001278916.2:c.902A>G