Canonical Allele Identifier: PA658661125
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 456144

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Arg318Met
CA8252614
NM_000135.4:c.953G>T