Canonical Allele Identifier: PA319969
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 213185
ClinVar RCV Id: RCV000195606 RCV000627831
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000492.2:p.Met1Thr