Canonical Allele Identifier: PA2826614986
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 1312158

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265841.1:p.Ala99Thr
CA4292419
NM_001278912.2:c.295G>A