Canonical Allele Identifier: PA2827383059
Gene: SGCE HGNC NCBI
ClinVar RCV:
RCV000388028
ClinVar Variation:
360988
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333646.1:p.Arg342Gln
CA4348674
NM_001346717.1:c.1025G>A