Canonical Allele Identifier: PA658680286
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 485556
ClinVar RCV Id: RCV000564564 RCV000705539 RCV001529212 RCV001821687
ClinVar Variation Id: 1047745
ClinVar RCV Id: RCV001352503 RCV002547560 RCV003339610
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Asp216Glu
CA1478642
NM_000143.4:c.648T>A
CA345439317
NM_000143.4:c.648T>G