ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA916063706
Gene: FANCI
HGNC
NCBI
Linked Data
ClinVar Variation Id:
435162
ClinVar RCV Id:
RCV000499688
RCV000550556
RCV001293992
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_060663.2:p.Arg959Trp
CA7723566
NM_018193.3:c.2875C>T