Canonical Allele Identifier: PA2825481483
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 213192

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075221.1:p.Gly206Val
CA324493
NM_001081752.3:c.617G>T