Canonical Allele Identifier: PA2499228994
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 1009323
ClinVar RCV Id: RCV002544999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Asn150Asp
CA345440085
NM_000143.4:c.448A>G