Canonical Allele Identifier: PA2825055030
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1399364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Ala1399Val
CA397483613
NM_000135.4:c.4196C>T