Canonical Allele Identifier: PA2826865252
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 581767
ClinVar RCV Id: RCV000705683
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288068.1:p.Gln388Glu
CA162911744
NM_001301139.2:c.1162C>G