Canonical Allele Identifier: PA2826615833
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 1312158

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265843.1:p.Ala89Thr
CA4292419
NM_001278914.2:c.265G>A