Allele Registry

Canonical Allele Identifier: PA110692

Gene: FANCA HGNC NCBI

ClinVar Allele:

213232

ClinVar RCV:

RCV000199923

RCV000674142

RCV001091062

RCV002252053

ClinVar Variation:

215981

HGVS (amino-acid)	Matching Registered Transcripts
NP_000126.2:p.Gln869Pro	CA338977 NM_000135.4:c.2606A>C