Canonical Allele Identifier: PA645431668
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 304204
ClinVar RCV Id: RCV000337238 RCV001094016 RCV001820899 RCV003967873
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Pro117Leu
CA5924363
NM_022725.4:c.350C>T