Canonical Allele Identifier: PA916029011
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 373239
ClinVar RCV Id: RCV000413165 RCV003505108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333642.1:p.Pro473Leu
CA4348533
NM_001346713.1:c.1418C>T