Canonical Allele Identifier: PA2573095352
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 1341334
ClinVar RCV Id: RCV001834547 RCV002542776
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Pro117Ser
CA5924365
NM_022725.4:c.349C>T