Canonical Allele Identifier: PA658803369
Gene: SGCB HGNC NCBI

Linked Data

ClinVar Variation Id: 534948
ClinVar RCV Id: RCV000642670 RCV001726283
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000223.1:p.Tyr184Cys
CA356876804
NM_000232.5:c.551A>G