Canonical Allele Identifier: PA187932
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 184137
ClinVar RCV Id: RCV000163293 RCV000467508 RCV001532106 RCV002291575 RCV004555540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Val73Met
CA187930
NM_000143.4:c.217G>A