Canonical Allele Identifier: PA915960474
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 640209
ClinVar RCV Id: RCV002536952
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Pro63Ser
CA345441892
NM_000143.4:c.187C>T