Canonical Allele Identifier: PA2826616143
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 360658

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265843.1:p.Leu585Phe
CA4293244
NM_001278914.2:c.1753C>T