Canonical Allele Identifier: PA159345
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134280

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Leu1339Phe
CA159343
NM_000135.4:c.4015C>T