Allele Registry

Canonical Allele Identifier: PA2826616839

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV003631356

ClinVar Variation:

2778493

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265845.1:p.Gly258Arg	CA4292716 NM_001278916.2:c.772G>A CA367870960 NM_001278916.2:c.772G>C