Canonical Allele Identifier: PA2826615468
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 450301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265842.1:p.Ala146Val
CA4292521
NM_001278913.2:c.437C>T