Allele Registry

Canonical Allele Identifier: PA2825481963

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV003631356

ClinVar Variation:

2778493

HGVS (amino-acid)	Matching Registered Transcripts
NP_001075222.1:p.Gly277Arg	CA4292716 NM_001081753.3:c.829G>A CA367870960 NM_001081753.3:c.829G>C