Allele Registry

Canonical Allele Identifier: PA645383042

Gene: FH HGNC NCBI

ClinVar Allele:

238257

ClinVar RCV:

RCV000230405

RCV001589168

RCV002372248

RCV002487046

ClinVar Variation:

237119

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Pro309Leu	CA1478570 NM_000143.4:c.926C>T