Canonical Allele Identifier: PA916010607
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 423742
ClinVar RCV Id: RCV000478684 RCV002470874 RCV002526957 RCV002525947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265868.1:p.Val542Ile
CA4293089
NM_001278939.2:c.1624G>A