Canonical Allele Identifier: PA2825329038
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 321371

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018122.1:p.Ser119Cys
CA8253054
NM_001018112.2:c.356C>G