Canonical Allele Identifier: PA2829454184
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 1719265
ClinVar RCV Id: RCV002302025
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003910.1:p.Glu379Lys
CA4348622
NM_003919.3:c.1135G>A