Allele Registry

Canonical Allele Identifier: PA916014939

Gene: FANCA HGNC NCBI

ClinVar Allele:

137990

ClinVar RCV:

RCV000120924

RCV000233082

RCV001333235

RCV002225374

RCV003952596

ClinVar Variation:

134251

HGVS (amino-acid)	Matching Registered Transcripts
NP_001273096.1:p.Lys701Glu	CA159266 NM_001286167.3:c.2101A>G