Canonical Allele Identifier: PA2825051710
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1053297
ClinVar RCV Id: RCV001361622

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Ser120Arg
CA286608257
NM_000135.4:c.360C>A
CA397480976
NM_000135.4:c.360C>G
CA397480980
NM_000135.4:c.358A>C