Canonical Allele Identifier: PA645404393
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 408205

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Arg1053Cys
CA8251319
NM_000135.4:c.3157C>T