Canonical Allele Identifier: PA2826865218
Gene: SGCE HGNC NCBI
ClinVar RCV:
RCV001373249
ClinVar Variation:
1063416
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288068.1:p.Pro358Ala
CA162920306
NM_001301139.2:c.1072C>G