Canonical Allele Identifier: PA2825328999
Gene: FANCA HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018122.1:p.His89Tyr
CA8253102
NM_001018112.2:c.265C>T