Canonical Allele Identifier: PA2825666853
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 1060764
ClinVar RCV Id: RCV001370234 RCV003234056 RCV001799074
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121681.1:p.Lys91Gln
CA362008093
NM_001128209.2:c.271A>C