Allele Registry

Canonical Allele Identifier: PA2826615940

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV003631356

ClinVar Variation:

2778493

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265843.1:p.Gly267Arg	CA4292716 NM_001278914.2:c.799G>A CA367870960 NM_001278914.2:c.799G>C