Canonical Allele Identifier: PA915960591
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 662672
ClinVar RCV Id: RCV002363155 RCV002537466
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Ile228Thr
CA345439247
NM_000143.4:c.683T>C