Canonical Allele Identifier: PA891852030
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 581767
ClinVar RCV Id: RCV000705683
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003910.1:p.Gln429Glu
CA162911744
NM_003919.3:c.1285C>G