Canonical Allele Identifier: PA2825329050
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134276
ClinVar RCV Id: RCV000120949

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018122.1:p.Ile124Phe
CA159331
NM_001018112.2:c.370A>T