Canonical Allele Identifier: PA916014881
Gene: FANCA HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Pro497Ser
CA16607150
NM_001286167.3:c.1489C>T