Canonical Allele Identifier: PA2580456733
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 2158805
ClinVar RCV Id: RCV003079925
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Asn149Asp
CA380059038
NM_022725.4:c.445A>G