Canonical Allele Identifier: PA2827382711
Gene: SGCE HGNC NCBI
ClinVar RCV:
RCV000803351
ClinVar Variation:
648594
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333644.1:p.Asn432Ser
CA368228891
NM_001346715.1:c.1295A>G