Canonical Allele Identifier: PA2825481415
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 1312158

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075221.1:p.Ala89Thr
CA4292419
NM_001081752.3:c.265G>A