Allele Registry

Canonical Allele Identifier: PA194348

Gene: FH HGNC NCBI

ClinVar RCV:

RCV000165850

RCV001557300

RCV003454408

ClinVar Variation:

186284

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.His135Arg	CA194346 NM_000143.4:c.404A>G