Canonical Allele Identifier: PA2573079673
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 306574
ClinVar RCV Id: RCV000268409
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373268.1:p.Ala1867Thr
CA10631790
NM_001386339.1:c.5599G>A