Allele Registry

Canonical Allele Identifier: PA246536

Gene: FH HGNC NCBI

ClinVar RCV:

RCV000442479

RCV000445630

RCV000493248

ClinVar Variation:

198045

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Ala298Pro	CA246534 NM_000143.4:c.892G>C