Allele Registry

Canonical Allele Identifier: PA645383190

Gene: FH HGNC NCBI

ClinVar RCV:

RCV000445626

RCV002525531

ClinVar Variation:

393578

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Asn373Ser	CA16609362 NM_000143.4:c.1118A>G