Canonical Allele Identifier: PA2826617851
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 524219
ClinVar RCV Id: RCV000627827 RCV000762455 RCV000765973 RCV002533162 RCV004533301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265847.1:p.Val470Ile
CA4293156
NM_001278918.2:c.1408G>A