Canonical Allele Identifier: PA2828687703
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 238309
ClinVar RCV Id: RCV000228956 RCV000482252 RCV000766508 RCV001094276 RCV003955318
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363839.1:p.Met432Val
CA7723058
NM_001376910.1:c.1294A>G