Canonical Allele Identifier: PA2829454151
Gene: SGCE HGNC NCBI
ClinVar RCV:
RCV002824246
ClinVar Variation:
2000060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003910.1:p.Met351Thr
CA368229612
NM_003919.3:c.1052T>C