Canonical Allele Identifier: PA189290
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 184555
ClinVar RCV Id: RCV000163828 RCV000195694 RCV003467282 RCV002498811 RCV003316008
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Thr234Ala
CA189288
NM_000143.4:c.700A>G