Canonical Allele Identifier: PA2499249956
Gene: SGCE HGNC NCBI
ClinVar RCV:
RCV001368574
ClinVar Variation:
1059320
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333642.1:p.Pro436Ser
CA368228928
NM_001346713.1:c.1306C>T