Canonical Allele Identifier: PA2499228995
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 1039915
ClinVar RCV Id: RCV002546990
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Asn150His
CA345440086
NM_000143.4:c.448A>C