Canonical Allele Identifier: PA2825202596
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 524218
ClinVar RCV Id: RCV000627826
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000492.2:p.Lys315Arg
CA367871485
NM_000501.4:c.944A>G