Canonical Allele Identifier: PA916014861
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 408183

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Arg435His
CA16615049
NM_001286167.3:c.1304G>A