Allele Registry

Canonical Allele Identifier: PA891845543

Gene: FH HGNC NCBI

ClinVar RCV:

RCV000701529

ClinVar Variation:

578504

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Asn373Ile	CA345437664 NM_000143.4:c.1118A>T