Canonical Allele Identifier: PA2825666841
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 202090
ClinVar RCV Id: RCV000183904
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121681.1:p.Gly80del
CA308794
NM_001128209.2:c.239_241del