Canonical Allele Identifier: PA2573203415
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_001333644.1:p.Ser361Leu
CA162922119
NM_001346715.1:c.1082C>T