Canonical Allele Identifier: PA2825481891
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 449781

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075222.1:p.Val159Met
CA4292496
NM_001081753.3:c.475G>A