Canonical Allele Identifier: PA2829111234
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 306600
ClinVar RCV Id: RCV001352894 RCV000547373 RCV000658587 RCV001002506 RCV002429258
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373271.1:p.Gln690Glu
CA5881611
NM_001386342.1:c.2068C>G