Canonical Allele Identifier: PA2826616750
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 213171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265845.1:p.Gly109Asp
CA320313
NM_001278916.2:c.326G>A