Canonical Allele Identifier: PA2499300213
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 1060764
ClinVar RCV Id: RCV001370234 RCV003234056 RCV001799074
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_758447.1:p.Lys92Gln
CA362008093
NM_172244.3:c.274A>C