Canonical Allele Identifier: PA159745
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 134416
ClinVar RCV Id: RCV000121092 RCV000575122 RCV001061733 RCV001558721
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Amino-acid Alleles

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