Canonical Allele Identifier: PA2499245741
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1063615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Pro1378Leu
CA8250776
NM_001286167.3:c.4133C>T