Canonical Allele Identifier: PA915969768
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 450301
ClinVar RCV Id: RCV000521003 RCV001161669 RCV002525163 RCV001161668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075223.1:p.Ala163Val
CA4292521
NM_001081754.3:c.488C>T