Allele Registry

Canonical Allele Identifier: PA2826617225

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV000486139

ClinVar Variation:

419450

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265846.1:p.Pro201Ser	CA16618557 NM_001278917.2:c.601C>T