Allele Registry

Canonical Allele Identifier: PA2741813258

Gene: FH HGNC NCBI

ClinVar RCV:

RCV003676763

RCV004371631

ClinVar Variation:

2805452

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Ser419Ala	CA345436877 NM_000143.4:c.1255T>G