Canonical Allele Identifier: PA916031221
Gene: FANCA HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338759.1:p.His89Tyr
CA8253102
NM_001351830.2:c.265C>T