Canonical Allele Identifier: PA2826615868
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 449781

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265843.1:p.Val149Met
CA4292496
NM_001278914.2:c.445G>A