Canonical Allele Identifier: PA2825481690
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 524219

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075221.1:p.Val530Ile
CA4293156
NM_001081752.3:c.1588G>A