Canonical Allele Identifier: PA2829454219
Gene: SGCE HGNC NCBI
ClinVar RCV:
RCV000803351
ClinVar Variation:
648594
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003910.1:p.Asn405Ser
CA368228891
NM_003919.3:c.1214A>G