Allele Registry

Canonical Allele Identifier: PA159748

Gene: FH HGNC NCBI

ClinVar RCV:

RCV000121093

RCV000554866

RCV000567053

RCV002514641

ClinVar Variation:

134417

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Met380Val	CA159746 NM_000143.4:c.1138A>G