Canonical Allele Identifier: PA2826615701
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 360658

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265842.1:p.Leu528Phe
CA4293244
NM_001278913.2:c.1582C>T