Canonical Allele Identifier: PA2825482651
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 450301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075224.1:p.Ala158Val
CA4292521
NM_001081755.3:c.473C>T