Canonical Allele Identifier: PA2826618239
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 360636
ClinVar RCV Id: RCV000327769 RCV000382394 RCV000492857 RCV000984480 RCV004530459
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265868.1:p.Ala110Thr
CA4292446
NM_001278939.2:c.328G>A