Canonical Allele Identifier: PA2826615905
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 213192

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265843.1:p.Gly211Val
CA324493
NM_001278914.2:c.632G>T