ClinGen Allele Registry
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Canonical Allele Identifier:
PA2828687393
Gene: FANCI
HGNC
NCBI
Linked Data
ClinVar Variation Id:
221078
ClinVar RCV Id:
RCV000205204
RCV001115870
RCV001804945
RCV003401110
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001363839.1:p.Glu3Lys
CA349390
NM_001376910.1:c.7G>A