Canonical Allele Identifier: PA658665589
Gene: SGCE HGNC NCBI
ClinVar RCV:
RCV000557233
ClinVar Variation:
464156
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003910.1:p.Pro157Leu
CA4348786
NM_003919.3:c.470C>T