ClinGen Allele Registry
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Canonical Allele Identifier:
PA2573074130
Gene: FANCI
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000001023
ClinVar Variation:
972
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001363840.1:p.Arg1285Gln
CA251642
NM_001376911.1:c.3854G>A