Allele Registry

Canonical Allele Identifier: PA215565

Gene: FH HGNC NCBI

ClinVar RCV:

RCV000034486

RCV000471678

RCV000568576

ClinVar Variation:

41584

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Leu303Ser	CA215563 NM_000143.4:c.908T>C