Allele Registry

Canonical Allele Identifier: PA2826617662

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV000486139

ClinVar Variation:

419450

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265847.1:p.Pro167Ser	CA16618557 NM_001278918.2:c.499C>T