Canonical Allele Identifier: PA2573074092
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 238321

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363839.1:p.Thr986Met
CA7723642
NM_001376910.1:c.2957C>T