Canonical Allele Identifier: PA2828066315
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 1413798
ClinVar RCV Id: RCV001928316
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349736.1:p.Ser296Leu
CA162922119
NM_001362807.2:c.887C>T