Canonical Allele Identifier: PA916010628
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 360660
ClinVar RCV Id: RCV000298998 RCV000407993 RCV001198806 RCV004544697
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265868.1:p.Ala699Thr
CA4293282
NM_001278939.2:c.2095G>A