Canonical Allele Identifier: PA645412469
Gene: SGCB HGNC NCBI

Linked Data

ClinVar Variation Id: 286721
ClinVar RCV Id: RCV000391362 RCV002519253
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000223.1:p.Arg223His
CA2918323
NM_000232.5:c.668G>A