Canonical Allele Identifier: PA2826710757
Gene: FANCA HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.His89Tyr
CA8253102
NM_001286167.3:c.265C>T