Canonical Allele Identifier: PA916014977
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 237040

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Ile865Val
CA10583438
NM_001286167.3:c.2593A>G