Allele Registry

Canonical Allele Identifier: PA658801124

Gene: FH HGNC NCBI

ClinVar Allele:

515718

ClinVar RCV:

RCV000635286

ClinVar Variation:

529802

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Cys377Tyr	CA345437584 NM_000143.4:c.1130G>A