Canonical Allele Identifier: PA2826617731
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 524218
ClinVar RCV Id: RCV000627826
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265847.1:p.Lys271Arg
CA367871485
NM_001278918.2:c.812A>G