Allele Registry

Canonical Allele Identifier: PA189213

Gene: FH HGNC NCBI

ClinVar Allele:

51260

ClinVar RCV:

RCV000034920

RCV000163798

RCV000199873

RCV001762109

RCV002280864

ClinVar Variation:

42094

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Gln376Pro	CA189211 NM_000143.4:c.1127A>C