Allele Registry

Canonical Allele Identifier: PA167339

Gene: FH HGNC NCBI

ClinVar Allele:

151789

ClinVar RCV:

RCV000130897

RCV000477037

RCV000765096

RCV001547779

RCV001731390

RCV004555538

ClinVar Variation:

142075

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Ala194Thr	CA167337 NM_000143.4:c.580G>A