Allele Registry

Canonical Allele Identifier: PA645382881

Gene: FH HGNC NCBI

ClinVar RCV:

RCV000445621

RCV003574775

ClinVar Variation:

393569

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.His235Asp	CA16609371 NM_000143.4:c.703C>G