Canonical Allele Identifier: PA2825481711
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 2613731
ClinVar RCV Id: RCV003384520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075221.1:p.Ala568Val
CA367889266
NM_001081752.3:c.1703C>T