Canonical Allele Identifier: PA2826617164
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 213171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265846.1:p.Gly99Asp
CA320313
NM_001278917.2:c.296G>A