Canonical Allele Identifier: PA2829111747
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 397621
ClinVar RCV Id: RCV000449588 RCV000498336 RCV000513369 RCV000626094 RCV000540860 RCV002339104
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373271.1:p.Lys1629del
CA5880839
NM_001386342.1:c.4885_4887del
CA379632617
NM_001386342.1:c.4884_4886del