Allele Registry

Canonical Allele Identifier: PA658680498

Gene: FH HGNC NCBI

ClinVar Allele:

448005

ClinVar RCV:

RCV000550902

RCV001011420

RCV002254703

RCV002527721

ClinVar Variation:

460342

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Lys470Glu	CA40371763 NM_000143.4:c.1408A>G