Allele Registry

Canonical Allele Identifier: PA915969784

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV000486139

ClinVar Variation:

419450

HGVS (amino-acid)	Matching Registered Transcripts
NP_001075223.1:p.Pro216Ser	CA16618557 NM_001081754.3:c.646C>T