Allele Registry

Canonical Allele Identifier: PA257463

Gene: FH HGNC NCBI

ClinVar RCV:

RCV000017624

RCV001781272

RCV002362588

ClinVar Variation:

16237

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Arg233Leu	CA257461 NM_000143.4:c.698G>T