Canonical Allele Identifier: PA658675573
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 450301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000492.2:p.Ala158Val
CA4292521
NM_000501.4:c.473C>T