Canonical Allele Identifier: PA2741860112
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_001333644.1:p.Arg326Gly
CA4348701
NM_001346715.1:c.976C>G