Canonical Allele Identifier: PA2825051743
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1957417
ClinVar RCV Id: RCV002690607

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Glu130Asp
CA8253040
NM_000135.4:c.390G>C
CA8253041
NM_000135.4:c.390G>T