Canonical Allele Identifier: PA2829111822
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2108417
ClinVar RCV Id: RCV003034163
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373271.1:p.Ala1757Asp
CA379630256
NM_001386342.1:c.5270C>A