Allele Registry

Canonical Allele Identifier: PA645382528

Gene: FH HGNC NCBI

ClinVar RCV:

RCV000467729

RCV000568361

RCV001530785

ClinVar Variation:

405936

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Arg87Cys	CA1478738 NM_000143.4:c.259C>T