Canonical Allele Identifier: PA658680378
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 460382
ClinVar RCV Id: RCV001097195 RCV000540225 RCV000569138 RCV001731756 RCV002490990
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Val306Ala
CA1478573
NM_000143.4:c.917T>C