Canonical Allele Identifier: PA2826616352
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 213192

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265844.1:p.Gly216Val
CA324493
NM_001278915.2:c.647G>T