Canonical Allele Identifier: PA645432853
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 429705
ClinVar RCV Id: RCV000512804 RCV002524034 RCV003323569
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265868.1:p.Gly473Asp
CA4292991
NM_001278939.2:c.1418G>A