Allele Registry

Canonical Allele Identifier: PA174972

Gene: SBF1 HGNC NCBI

ClinVar RCV:

RCV000149508

RCV000162103

ClinVar Variation:

162096

HGVS (amino-acid)	Matching Registered Transcripts
NP_002963.2:p.Asp443Asn	CA174971 NM_002972.4:c.1327G>A