Allele Registry

Canonical Allele Identifier: PA3057517378

Gene: FH HGNC NCBI

ClinVar RCV:

RCV005167903

ClinVar Variation:

3690088

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Pro174Leu	CA345439915 NM_000143.4:c.521C>T