Canonical Allele Identifier: PA2826710812
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1053297
ClinVar RCV Id: RCV001361622
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Ser120Arg
CA286608257
NM_001286167.3:c.360C>A
CA397480976
NM_001286167.3:c.360C>G
CA397480980
NM_001286167.3:c.358A>C