Canonical Allele Identifier: PA2825481928
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 213192

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075222.1:p.Gly221Val
CA324493
NM_001081753.3:c.662G>T