Canonical Allele Identifier: PA645383097
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 393575
ClinVar RCV Id: RCV000445616 RCV002525530 RCV004555576
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Asp341Gly
CA16609365
NM_000143.4:c.1022A>G