Canonical Allele Identifier: PA2825666830
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 907807
ClinVar RCV Id: RCV001157912
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121681.1:p.Leu69Pro
CA362007952
NM_001128209.2:c.206T>C