Canonical Allele Identifier: PA2825054085
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 2984181
ClinVar RCV Id: RCV003843340

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Glu918Gln
CA397438008
NM_000135.4:c.2752G>C