ClinGen Allele Registry
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Canonical Allele Identifier:
PA2829111111
Gene: SBF2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
306606
ClinVar RCV Id:
RCV000654076
RCV001172806
RCV001094221
RCV002392844
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001373271.1:p.Glu464Lys
CA5881810
NM_001386342.1:c.1390G>A