Canonical Allele Identifier: PA2825054875
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 998617
ClinVar RCV Id: RCV001294503

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Arg1321Pro
CA397484830
NM_000135.4:c.3962G>C