Canonical Allele Identifier: PA915969784
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 419450
ClinVar RCV Id: RCV000486139
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075223.1:p.Pro216Ser
CA16618557
NM_001081754.3:c.646C>T