Allele Registry

Canonical Allele Identifier: PA2826615020

Gene: ELN HGNC NCBI

ClinVar Allele:

444158

ClinVar RCV:

RCV000521003

RCV001161668

RCV001161669

RCV002525163

ClinVar Variation:

450301

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265841.1:p.Ala158Val	CA4292521 NM_001278912.2:c.473C>T