Canonical Allele Identifier: PA2826615309
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 360658

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265841.1:p.Leu609Phe
CA4293244
NM_001278912.2:c.1825C>T