Canonical Allele Identifier: PA340755
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 8174
ClinVar RCV Id: RCV000008652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000328.2:p.Glu262Lys
CA340753
NM_000337.6:c.784G>A