Allele Registry

Canonical Allele Identifier: PA2825481518

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV003631356

ClinVar Variation:

2778493

HGVS (amino-acid)	Matching Registered Transcripts
NP_001075221.1:p.Gly262Arg	CA4292716 NM_001081752.3:c.784G>A CA367870960 NM_001081752.3:c.784G>C