Allele Registry

Canonical Allele Identifier: PA159745

Gene: FH HGNC NCBI

ClinVar Allele:

138155

ClinVar RCV:

RCV000121092

RCV000575122

RCV001061733

RCV001558721

ClinVar Variation:

134416

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Ile338Thr	CA159743 NM_000143.4:c.1013T>C