Allele Registry

Canonical Allele Identifier: PA3057494880

Gene: FH HGNC NCBI

ClinVar RCV:

RCV005125387

ClinVar Variation:

3650033

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Glu404Lys	CA345437313 NM_000143.4:c.1210G>A