Allele Registry

Canonical Allele Identifier: PA658801094

Gene: FH HGNC NCBI

ClinVar RCV:

RCV002386008

RCV003539990

ClinVar Variation:

529822

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Leu244Pro	CA345439154 NM_000143.4:c.731T>C