Canonical Allele Identifier: PA2573095356
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 1319635
ClinVar RCV Id: RCV001861121 RCV003237628
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.His267Gln
CA5924257
NM_022725.4:c.801C>G
CA5924258
NM_022725.4:c.801C>A