Canonical Allele Identifier: PA1139754461
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 854237
ClinVar RCV Id: RCV001059241
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Ile293Val
CA5924239
NM_022725.4:c.877A>G