Allele Registry

Canonical Allele Identifier: PA159751

Gene: FH HGNC NCBI

ClinVar RCV:

RCV000121094

RCV000473170

RCV000571469

RCV001564388

RCV003325184

RCV004555537

ClinVar Variation:

134418

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Val435Met	CA159749 NM_000143.4:c.1303G>A