Canonical Allele Identifier: PA916063496
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 456223

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060663.2:p.Met201Val
CA7722697
NM_018193.3:c.601A>G