Allele Registry

Canonical Allele Identifier: PA285324

Gene: FH HGNC NCBI

ClinVar RCV:

RCV000078144

RCV000445624

RCV000492881

RCV004555536

ClinVar Variation:

92451

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Ser419Pro	CA285322 NM_000143.4:c.1255T>C