Canonical Allele Identifier: PA1139754469
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 964280
ClinVar RCV Id: RCV001238473 RCV001788429
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Trp304Ser
CA5924232
NM_022725.4:c.911G>C