Canonical Allele Identifier: PA2580111045
Gene: SGCB HGNC NCBI

Linked Data

ClinVar Variation Id: 2435898
ClinVar RCV Id: RCV003136648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000223.1:p.Asp215Val
CA356876222
NM_000232.5:c.644A>T