Canonical Allele Identifier: PA658801041
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 529819
ClinVar RCV Id: RCV000635308 RCV002325224 RCV002509481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Leu14Phe
CA40338036
NM_000143.4:c.40C>T