Canonical Allele Identifier: PA2826615465
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 449781

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265842.1:p.Val142Met
CA4292496
NM_001278913.2:c.424G>A