Canonical Allele Identifier: PA915966371
Gene: SGCB HGNC NCBI

Linked Data

ClinVar Variation Id: 650059
ClinVar RCV Id: RCV000805140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000223.1:p.Phe233Ser
CA356875860
NM_000232.5:c.698T>C