Canonical Allele Identifier: PA2826616555
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 423742

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265844.1:p.Val519Ile
CA4293089
NM_001278915.2:c.1555G>A