Canonical Allele Identifier: PA645431692
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 408148
ClinVar RCV Id: RCV000457751 RCV002506120
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Asn149Ser
CA5924330
NM_022725.4:c.446A>G