Canonical Allele Identifier: PA2825481478
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 419450
ClinVar RCV Id: RCV000486139

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075221.1:p.Pro201Ser
CA16618557
NM_001081752.3:c.601C>T