Canonical Allele Identifier: PA645412455
Gene: SGCB HGNC NCBI

Linked Data

ClinVar Variation Id: 284136
ClinVar RCV Id: RCV000400638 RCV001247007
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000223.1:p.Asn140Ser
CA2918415
NM_000232.5:c.419A>G