Canonical Allele Identifier: PA2826615439
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 213171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265842.1:p.Gly97Asp
CA320313
NM_001278913.2:c.290G>A