Canonical Allele Identifier: PA2741850066
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 2984539
ClinVar RCV Id: RCV003845682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265868.1:p.Gly80Ser
CA4292406
NM_001278939.2:c.238G>A