Canonical Allele Identifier: PA916010618
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 360658

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265868.1:p.Leu671Phe
CA4293244
NM_001278939.2:c.2011C>T