Canonical Allele Identifier: PA2825536835
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 1722976
ClinVar RCV Id: RCV002306083 RCV003138163
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092871.1:p.Gly293Ala
CA368231184
NM_001099401.2:c.878G>C