Allele Registry

Canonical Allele Identifier: PA355857

Gene: FANCG HGNC NCBI

ClinVar RCV:

RCV000205598

RCV000502118

RCV001449943

RCV002515531

RCV003237771

ClinVar Variation:

221037

HGVS (amino-acid)	Matching Registered Transcripts
NP_004620.1:p.Pro241Leu	CA349730 NM_004629.2:c.722C>T