Canonical Allele Identifier: PA916029016
Gene: SGCE HGNC NCBI
ClinVar RCV:
RCV000006129
ClinVar Variation:
5773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333644.1:p.Leu232Arg
CA253601
NM_001346715.1:c.695T>G