Canonical Allele Identifier: PA2825666904
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 959625
ClinVar RCV Id: RCV001233009 RCV003166428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121681.1:p.Val140Leu
CA362010420
NM_001128209.2:c.418G>C
CA362010422
NM_001128209.2:c.418G>T