Canonical Allele Identifier: PA645412473
Gene: SGCB HGNC NCBI

Linked Data

ClinVar Variation Id: 283043
ClinVar RCV Id: RCV000284183 RCV000295248 RCV000386817 RCV000534489 RCV000852968
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000223.1:p.Arg267Cys
CA2918272
NM_000232.5:c.799C>T