Allele Registry

Canonical Allele Identifier: PA645382903

Gene: FH HGNC NCBI

ClinVar RCV:

RCV000445612

RCV003168712

RCV003558385

ClinVar Variation:

393571

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Leu244Arg	CA16609370 NM_000143.4:c.731T>G