Canonical Allele Identifier: PA2829454216
Gene: SGCE HGNC NCBI
ClinVar RCV:
RCV001368574
ClinVar Variation:
1059320
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003910.1:p.Pro400Ser
CA368228928
NM_003919.3:c.1198C>T