Allele Registry

Canonical Allele Identifier: PA2826615089

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV003631356

ClinVar Variation:

2778493

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265841.1:p.Gly272Arg	CA4292716 NM_001278912.2:c.814G>A CA367870960 NM_001278912.2:c.814G>C