Canonical Allele Identifier: PA645383034
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 405930
ClinVar RCV Id: RCV000571863 RCV001591074
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Pro309Ser
CA1478571
NM_000143.4:c.925C>T