Canonical Allele Identifier: PA658661859
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 456284
ClinVar RCV Id: RCV000764967 RCV000557500 RCV001545711 RCV001821485 RCV002527669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Ser191Arg
CA5924307
NM_022725.4:c.573C>A
CA5924308
NM_022725.4:c.573C>G
CA380058772
NM_022725.4:c.571A>C