Canonical Allele Identifier: PA2826617327
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 1437068
ClinVar RCV Id: RCV001955408 RCV002484677 RCV003107902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265846.1:p.Gly374Arg
CA4292860
NM_001278917.2:c.1120G>A
CA367881568
NM_001278917.2:c.1120G>C