Allele Registry

Canonical Allele Identifier: PA112055

Gene: FH HGNC NCBI

ClinVar RCV:

RCV000017620

RCV000078148

RCV000493777

ClinVar Variation:

92455

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Asn107Thr	CA257456 NM_000143.4:c.320A>C