Canonical Allele Identifier: PA645412408
Gene: SGCB HGNC NCBI

Linked Data

ClinVar Variation Id: 282248
ClinVar RCV Id: RCV000261367 RCV000399677 RCV000543057 RCV002229741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000223.1:p.Gln11Glu
CA2918525
NM_000232.5:c.31C>G