Canonical Allele Identifier: PA2825482685
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 213192

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075224.1:p.Gly216Val
CA324493
NM_001081755.3:c.647G>T