Canonical Allele Identifier: PA645405470
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 238321
ClinVar RCV Id: RCV000233382 RCV001119128 RCV003967621
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001106849.1:p.Thr1079Met
CA7723642
NM_001113378.1:c.3236C>T