Canonical Allele Identifier: PA2826616002
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 1437068

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265843.1:p.Gly379Arg
CA4292860
NM_001278914.2:c.1135G>A
CA367881568
NM_001278914.2:c.1135G>C