ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA916063521
Gene: FANCI
HGNC
NCBI
Linked Data
ClinVar Variation Id:
317269
ClinVar RCV Id:
RCV000294568
RCV001094369
RCV003920334
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_060663.2:p.Ser371Gly
CA7722914
NM_018193.3:c.1111A>G