Canonical Allele Identifier: PA2580206362
Gene: SGCE HGNC NCBI
ClinVar RCV:
RCV002302025
ClinVar Variation:
1719265
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333642.1:p.Glu415Lys
CA4348622
NM_001346713.1:c.1243G>A