Allele Registry

Canonical Allele Identifier: PA2826616811

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV000486139

ClinVar Variation:

419450

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265845.1:p.Pro211Ser	CA16618557 NM_001278916.2:c.631C>T