Canonical Allele Identifier: PA916029010
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 581767
ClinVar RCV Id: RCV000705683
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333642.1:p.Gln465Glu
CA162911744
NM_001346713.1:c.1393C>G