Canonical Allele Identifier: PA2826615151
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 1437068

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265841.1:p.Gly384Arg
CA4292860
NM_001278912.2:c.1150G>A
CA367881568
NM_001278912.2:c.1150G>C