Canonical Allele Identifier: PA2829111423
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 246062
ClinVar RCV Id: RCV000416078 RCV001114470 RCV001085919 RCV001172800 RCV001564019 RCV002321906 RCV003919998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373271.1:p.Thr1054Asn
CA5881312
NM_001386342.1:c.3161C>A