Canonical Allele Identifier: PA2826617871
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 1411399
ClinVar RCV Id: RCV001942947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265847.1:p.Gly507Glu
CA367889247
NM_001278918.2:c.1520G>A