Canonical Allele Identifier: PA2826617162
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 1312158
ClinVar RCV Id: RCV001761379 RCV003631222
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265846.1:p.Ala89Thr
CA4292419
NM_001278917.2:c.265G>A