Canonical Allele Identifier: PA321711
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 213166
ClinVar RCV Id: RCV000405378 RCV000351619 RCV001579602 RCV004530153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000492.2:p.Pro667Ser
CA321710
NM_000501.4:c.1999C>T