Canonical Allele Identifier: PA2825202387
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 1312158

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000492.2:p.Ala99Thr
CA4292419
NM_000501.4:c.295G>A