Canonical Allele Identifier: PA891845517
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 576598
ClinVar RCV Id: RCV000699131 RCV002534369
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Ile173Leu
CA345439924
NM_000143.4:c.517A>C
CA345439926
NM_000143.4:c.517A>T