Canonical Allele Identifier: PA2825482429
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 423742

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075223.1:p.Val518Ile
CA4293089
NM_001081754.3:c.1552G>A