Canonical Allele Identifier: PA159315
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134268

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Pro1175Leu
CA159313
NM_000135.4:c.3524C>T