Allele Registry

Canonical Allele Identifier: PA295618

Gene: FH HGNC NCBI

ClinVar RCV:

RCV000153234

RCV000217529

RCV000445620

ClinVar Variation:

167065

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Ala385Asp	CA295616 NM_000143.4:c.1154C>A