Allele Registry

Canonical Allele Identifier: PA915960603

Gene: FH HGNC NCBI

ClinVar RCV:

RCV001025872

RCV002551940

ClinVar Variation:

826742

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Arg233Gly	CA345439219 NM_000143.4:c.697C>G