Allele Registry

Canonical Allele Identifier: PA658680198

Gene: FH HGNC NCBI

ClinVar RCV:

RCV000549382

RCV002413481

RCV002528326

ClinVar Variation:

460347

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Asp65Asn	CA1478750 NM_000143.4:c.193G>A