Canonical Allele Identifier: PA2828689022
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 408251
ClinVar RCV Id: RCV000471427 RCV002481431
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363840.1:p.Ile735Thr
CA16614749
NM_001376911.1:c.2204T>C