Canonical Allele Identifier: PA2825133302
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 2237240
ClinVar RCV Id: RCV002723872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000328.2:p.Lys78Gln
CA362007998
NM_000337.6:c.232A>C