Canonical Allele Identifier: PA174972
Gene: SBF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 162096
ClinVar RCV Id: RCV000149508 RCV000162103
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Amino-acid Alleles

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