Canonical Allele Identifier: PA2580106846
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 1779932
ClinVar RCV Id: RCV002404041
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Glu59Asp
CA345441924
NM_000143.4:c.177A>T
CA345441926
NM_000143.4:c.177A>C