Canonical Allele Identifier: PA2826865184
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_001288068.1:p.Glu338Lys
CA4348622
NM_001301139.2:c.1012G>A