Canonical Allele Identifier: PA916015204
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134280

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Leu1339Phe
CA159343
NM_001286167.3:c.4015C>T