Allele Registry

Canonical Allele Identifier: PA341391

Gene: FH HGNC NCBI

ClinVar RCV:

RCV000017625

RCV000489422

RCV002433458

ClinVar Variation:

16238

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Arg101Pro	CA341389 NM_000143.4:c.302G>C