Allele Registry

Canonical Allele Identifier: PA257452

Gene: FH HGNC NCBI

ClinVar RCV:

RCV000017617

ClinVar Variation:

16230

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Ala265Thr	CA257450 NM_000143.4:c.793G>A