Allele Registry

Canonical Allele Identifier: PA2826615900

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV000486139

ClinVar Variation:

419450

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265843.1:p.Pro206Ser	CA16618557 NM_001278914.2:c.616C>T