Allele Registry

Canonical Allele Identifier: PA645383030

Gene: FH HGNC NCBI

ClinVar RCV:

RCV000430394

RCV001019060

ClinVar Variation:

392178

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Ala308Gly	CA16603595 NM_000143.4:c.923C>G