Canonical Allele Identifier: PA2826277687
Gene: ELOC HGNC NCBI

Linked Data

ClinVar Variation Id: 376556
ClinVar RCV Id: RCV000443719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191792.1:p.Tyr63Ser
CA16602982
NM_001204863.2:c.188A>C