ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA143930
Gene: SBF1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
51006
ClinVar RCV Id:
RCV000043694
RCV000762082
RCV002281731
RCV003318497
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_002963.2:p.Thr1590Ala
CA143929
NM_002972.4:c.4768A>G