Allele Registry

Canonical Allele Identifier: PA320606

Gene: FH HGNC NCBI

ClinVar RCV:

RCV000196179

RCV000220270

RCV000445606

ClinVar Variation:

214374

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Ser365Gly	CA320604 NM_000143.4:c.1093A>G