Allele Registry

Canonical Allele Identifier: PA320501

Gene: FH HGNC NCBI

ClinVar RCV:

RCV000196089

RCV000445631

RCV001019611

ClinVar Variation:

214417

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Val322Gly	CA320499 NM_000143.4:c.965T>G