Canonical Allele Identifier: PA2826277672
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_001191789.1:p.Tyr79Ser
CA16602982
NM_001204860.2:c.236A>C