Canonical Allele Identifier: PA2829110629
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 246062
ClinVar RCV Id: RCV000416078 RCV001114470 RCV001085919 RCV001172800 RCV001564019 RCV002321906 RCV003919998
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373268.1:p.Thr1097Asn
CA5881312
NM_001386339.1:c.3290C>A