Canonical Allele Identifier: PA2826617230
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 213192

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265846.1:p.Gly206Val
CA324493
NM_001278917.2:c.617G>T