Canonical Allele Identifier: PA2826615436
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 1312158

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265842.1:p.Ala87Thr
CA4292419
NM_001278913.2:c.259G>A