Canonical Allele Identifier: PA645431700
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 252737
ClinVar RCV Id: RCV000239026 RCV000320511 RCV001093961 RCV001358441
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Gln211His
CA5924296
NM_022725.4:c.633G>T
CA380058640
NM_022725.4:c.633G>C