Canonical Allele Identifier: PA916063574
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 238309

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060663.2:p.Met525Val
CA7723058
NM_018193.3:c.1573A>G