ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA645405070
Gene: FANCI
HGNC
NCBI
Linked Data
ClinVar Variation Id:
238307
ClinVar RCV Id:
RCV000515122
RCV001082996
RCV002500767
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001106849.1:p.Ile404Thr
CA7722946
NM_001113378.1:c.1211T>C