Canonical Allele Identifier: PA2826615906
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 213175

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265843.1:p.Pro215Leu
CA322484
NM_001278914.2:c.644C>T