ClinGen Allele Registry
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Canonical Allele Identifier:
PA2573079681
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_001373271.1:p.Gln976Leu
CA5881388
NM_001386342.1:c.2927A>T