Allele Registry

Canonical Allele Identifier: PA891845518

Gene: FH HGNC NCBI

ClinVar RCV:

RCV002533626

ClinVar Variation:

578513

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Pro174His	CA345439916 NM_000143.4:c.521C>A