Canonical Allele Identifier: PA645405152
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 414868
ClinVar RCV Id: RCV000466767 RCV001119038 RCV003401499 RCV003902684
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001106849.1:p.Gly655Arg
CA7723227
NM_001113378.1:c.1963G>A
CA393748775
NM_001113378.1:c.1963G>C