Canonical Allele Identifier: PA2826617667
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 213192

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265847.1:p.Gly172Val
CA324493
NM_001278918.2:c.515G>T