Allele Registry

Canonical Allele Identifier: PA916015020

Gene: FANCA HGNC NCBI

ClinVar Allele:

401422

ClinVar RCV:

RCV000466964

RCV000669024

ClinVar Variation:

408196

HGVS (amino-acid)	Matching Registered Transcripts
NP_001273096.1:p.Arg951Trp	CA8251482 NM_001286167.3:c.2851C>T