Canonical Allele Identifier: PA1139729182
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 938661
ClinVar RCV Id: RCV001207926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333642.1:p.Asn413His
CA4348623
NM_001346713.1:c.1237A>C