Canonical Allele Identifier: PA2829110584
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 448239
ClinVar RCV Id: RCV000516551 RCV001474077 RCV002448559 RCV003942700
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373268.1:p.Gln1019Leu
CA5881388
NM_001386339.1:c.3056A>T