Canonical Allele Identifier: PA2825328855
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 237054

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018122.1:p.Asp14Gly
CA8253266
NM_001018112.2:c.41A>G