Canonical Allele Identifier: PA2826616139
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 911325
ClinVar Variation Id: 1691674
ClinVar RCV Id: RCV002255080

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265843.1:p.Gly583Arg
CA4293241
NM_001278914.2:c.1747G>A
CA4293242
NM_001278914.2:c.1747G>C