Allele Registry

Canonical Allele Identifier: PA645472435

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV000486139

ClinVar Variation:

419450

HGVS (amino-acid)	Matching Registered Transcripts
NP_000492.2:p.Pro211Ser	CA16618557 NM_000501.4:c.631C>T