Allele Registry

Canonical Allele Identifier: PA197227

Gene: FH HGNC NCBI

ClinVar Allele:

181638

ClinVar RCV:

RCV000166997

RCV000469505

RCV001101030

RCV002516512

RCV003320130

ClinVar Variation:

187279

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Ile120Val	CA197225 NM_000143.4:c.358A>G