Allele Registry

Canonical Allele Identifier: PA2826617082

Gene: ELN HGNC NCBI

ClinVar Allele:

209939

ClinVar RCV:

RCV000351619

RCV000405378

RCV001579602

RCV004530153

ClinVar Variation:

213166

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265845.1:p.Pro619Ser	CA321710 NM_001278916.2:c.1855C>T