Canonical Allele Identifier: PA645404711
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 408170

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Arg1409Trp
CA8250683
NM_000135.4:c.4225C>T