Canonical Allele Identifier: PA2499289396
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 1001967
ClinVar RCV Id: RCV001298328 RCV002499547
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Tyr274Ser
CA5924254
NM_022725.4:c.821A>C