Canonical Allele Identifier: PA2825666901
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 1007737
ClinVar RCV Id: RCV001304964
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121681.1:p.Lys137Asn
CA362010378
NM_001128209.2:c.411A>C
CA362010380
NM_001128209.2:c.411A>T