Allele Registry

Canonical Allele Identifier: PA2825202727

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV003518218

ClinVar Variation:

2713291

HGVS (amino-acid)	Matching Registered Transcripts
NP_000492.2:p.Gln442Glu	CA367881956 NM_000501.4:c.1324C>G