Canonical Allele Identifier: PA2827382387
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 3160987
ClinVar RCV Id: RCV004455873
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333642.1:p.Arg326Cys
CA4348699
NM_001346713.1:c.976C>T