Canonical Allele Identifier: PA2499229881
Gene: SGCB HGNC NCBI

Linked Data

ClinVar Variation Id: 978759
ClinVar RCV Id: RCV001293214 RCV002222690
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000223.1:p.Ala9del
CA2670614613
NM_000232.5:c.24_26del