Canonical Allele Identifier: PA2825051728
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1692223
ClinVar RCV Id: RCV002257107

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Thr126Ser
CA397480946
NM_000135.4:c.376A>T