Canonical Allele Identifier: PA2827382929
Gene: SGCE HGNC NCBI
ClinVar RCV:
RCV000006129
ClinVar Variation:
5773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333646.1:p.Leu196Arg
CA253601
NM_001346717.1:c.587T>G