Allele Registry

Canonical Allele Identifier: PA2573162674

Gene: FH HGNC NCBI

ClinVar RCV:

RCV002592600

ClinVar Variation:

1489220

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Arg233Pro	CA345439218 NM_000143.4:c.698G>C