Canonical Allele Identifier: PA2826616604
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_001265844.1:p.Gly613Arg
CA4293241
NM_001278915.2:c.1837G>A
CA4293242
NM_001278915.2:c.1837G>C