Canonical Allele Identifier: PA2573079567
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 225095
ClinVar RCV Id: RCV000210630 RCV003743643
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373268.1:p.Val1318Ala
CA358114
NM_001386339.1:c.3953T>C