Canonical Allele Identifier: PA2827383659
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 2731847
ClinVar RCV Id: RCV003506461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333649.1:p.Arg199Gly
CA4348701
NM_001346720.2:c.595C>G