Allele Registry

Canonical Allele Identifier: PA891845523

Gene: FH HGNC NCBI

ClinVar RCV:

RCV002534328

ClinVar Variation:

574229

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Gln185Pro	CA345439820 NM_000143.4:c.554A>C