Canonical Allele Identifier: PA2828066373
Gene: SGCE HGNC NCBI
ClinVar RCV:
RCV001368574
ClinVar Variation:
1059320
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349736.1:p.Pro362Ser
CA368228928
NM_001362807.2:c.1084C>T