Canonical Allele Identifier: PA103346
Gene: SGCD HGNC NCBI
ClinVar RCV:
RCV000008652
ClinVar Variation:
8174
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121681.1:p.Glu261Lys
CA340753
NM_001128209.2:c.781G>A