Canonical Allele Identifier: PA2826618293
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 213175

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265868.1:p.Pro220Leu
CA322484
NM_001278939.2:c.659C>T