Allele Registry

Canonical Allele Identifier: PA658680376

Gene: FH HGNC NCBI

ClinVar RCV:

RCV000525503

RCV001545353

RCV002377041

ClinVar Variation:

460381

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Pro304Arg	CA1478574 NM_000143.4:c.911C>G