Allele Registry

Canonical Allele Identifier: PA325183

Gene: FH HGNC NCBI

ClinVar RCV:

RCV000200592

RCV001017278

RCV002291591

ClinVar Variation:

214419

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Ser366Asn	CA325181 NM_000143.4:c.1097G>A