Canonical Allele Identifier: PA658660457
Gene: SGCB HGNC NCBI

Linked Data

ClinVar Variation Id: 466605
ClinVar RCV Id: RCV000556382
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000223.1:p.Gly236Asp
CA356875836
NM_000232.5:c.707G>A