Allele Registry

Canonical Allele Identifier: PA645382481

Gene: FH HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

280166

627684

ClinVar RCV:

RCV000307949

RCV000369616

RCV000794812

RCV002418146

RCV002422699

RCV002522126

RCV002535910

ClinVar Variation:

296878

641546

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000134.2:p.Met1Leu