Canonical Allele Identifier: PA916063432
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 317258
ClinVar RCV Id: RCV000356939 RCV001344485
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060663.2:p.Arg66Cys
CA7722529
NM_018193.3:c.196C>T