Canonical Allele Identifier: PA2580111047
Gene: SGCB HGNC NCBI

Linked Data

ClinVar Variation Id: 2098233
ClinVar RCV Id: RCV003030838
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000223.1:p.Gly231Ser
CA356876001
NM_000232.5:c.691G>A