Canonical Allele Identifier: PA159301
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134263

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Gln993Lys
CA159299
NM_000135.4:c.2977C>A