Canonical Allele Identifier: PA916015008
Gene: FANCA HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Lys921Ile
CA10575737
NM_001286167.3:c.2762A>T