Canonical Allele Identifier: PA2826615579
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 2917076
ClinVar RCV Id: RCV003632903
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265842.1:p.Ala342Thr
CA367881526
NM_001278913.2:c.1024G>A