Canonical Allele Identifier: PA1139678255
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 964063
ClinVar RCV Id: RCV002567915 RCV003380923
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Ile52Val
CA345442002
NM_000143.4:c.154A>G