Canonical Allele Identifier: PA645412430
Gene: SGCB HGNC NCBI

Linked Data

ClinVar Variation Id: 284504
ClinVar RCV Id: RCV000261513
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000223.1:p.Cys67_Ile70del
CA10604820
NM_000232.5:c.199_210del