Canonical Allele Identifier: PA658661346
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 456207

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001106849.1:p.Gly79Glu
CA393738000
NM_001113378.1:c.236G>A