Canonical Allele Identifier: PA2827383716
Gene: SGCE HGNC NCBI
ClinVar RCV:
RCV002824246
ClinVar Variation:
2000060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333649.1:p.Met260Thr
CA368229612
NM_001346720.2:c.779T>C