Canonical Allele Identifier: PA2826615759
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 360661
ClinVar RCV Id: RCV000311994 RCV000369053 RCV000443075
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265842.1:p.Pro612Ser
CA4293372
NM_001278913.2:c.1834C>T