Allele Registry

Canonical Allele Identifier: PA658680414

Gene: FH HGNC NCBI

ClinVar RCV:

RCV000567804

RCV000635318

RCV000994324

ClinVar Variation:

485562

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Arg350Gln	CA1478555 NM_000143.4:c.1049G>A