Canonical Allele Identifier: PA2829898256
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 456219
ClinVar RCV Id: RCV000547520 RCV001194160 RCV003403255 RCV003979941
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060663.2:p.Ile1229Val
CA7723936
NM_018193.3:c.3685A>G