Canonical Allele Identifier: PA2828688128
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 435162
ClinVar RCV Id: RCV000499688 RCV000550556 RCV001293992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363839.1:p.Arg926Trp
CA7723566
NM_001376910.1:c.2776C>T