ClinGen Allele Registry
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Canonical Allele Identifier:
PA2573074097
Gene: FANCI
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
400530
ClinVar RCV:
RCV000463193
RCV001121010
RCV001821273
RCV003237865
RCV004022682
ClinVar Variation:
408253
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001363840.1:p.Asn836Ser
CA16614575
NM_001376911.1:c.2507A>G