Canonical Allele Identifier: PA891863653
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 591962
ClinVar RCV Id: RCV000723145 RCV002485842 RCV002535042
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Ala107Pro
CA5924375
NM_022725.4:c.319G>C
CA891862822
NM_022725.4:c.318_319delinsCC