Canonical Allele Identifier: PA112818
Gene: SGCB HGNC NCBI

Linked Data

ClinVar Variation Id: 499193
ClinVar RCV Id: RCV000596054 RCV000813259 RCV001267014 RCV001779022
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000223.1:p.Arg91Cys
CA2918445
NM_000232.5:c.271C>T