Canonical Allele Identifier: PA2825055026
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 2049844

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Lys1398Arg
CA397483646
NM_000135.4:c.4193A>G