Allele Registry

Canonical Allele Identifier: PA2741813097

Gene: FH HGNC NCBI

ClinVar RCV:

RCV003339134

ClinVar Variation:

2587063

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Ala298Ser	CA40328116 NM_000143.4:c.892G>T