Canonical Allele Identifier: PA2825536546
Gene: SGCE HGNC NCBI
ClinVar RCV:
RCV001368574
ClinVar Variation:
1059320
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092870.1:p.Pro391Ser
CA368228928
NM_001099400.2:c.1171C>T