Canonical Allele Identifier: PA915960559
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 825940
ClinVar RCV Id: RCV001024482 RCV001100768 RCV001098959 RCV002551893
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Pro192Ser
CA345439470
NM_000143.4:c.574C>T