Canonical Allele Identifier: PA2826614990
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 360636

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265841.1:p.Ala110Thr
CA4292446
NM_001278912.2:c.328G>A