Allele Registry

Canonical Allele Identifier: PA323996

Gene: FH HGNC NCBI

ClinVar RCV:

RCV000199454

RCV002257492

ClinVar Variation:

214376

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.His235Tyr	CA323994 NM_000143.4:c.703C>T