Canonical Allele Identifier: PA658818823
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 522334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Ile525Val
CA8252237
NM_001286167.3:c.1573A>G