Canonical Allele Identifier: PA2825666834
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 1789219
ClinVar RCV Id: RCV002457534
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121681.1:p.Leu76Ile
CA362007993
NM_001128209.2:c.226C>A